Human (GRCh38.p14)
Description

family with sequence similarity 66 member B [Source:HGNC Symbol;Acc:HGNC:28890]

Location
About this transcript

This transcript has 6 exons, is associated with 24386 variant alleles and maps to 741 oligo probes.

Gene
Transcript IDNamebpProteinTranslation IDBiotypeCCDSRefSeq MatchFlags
ENST00000653873.1FAM66B-2032209No protein-
 
Retained intron
--
ENST00000670717.1FAM66B-2092188No protein-
 
Retained intron
--
ENST00000664195.1FAM66B-2074238No protein-
 
lncRNA
-Ensembl Canonical
ENST00000663272.1FAM66B-2064350No protein-
 
lncRNA
-GENCODE basic
ENST00000665607.1FAM66B-2084069No protein-
 
lncRNA
--
ENST00000656213.1FAM66B-2044029No protein-
 
lncRNA
--
ENST00000656567.1FAM66B-2053774No protein-
 
lncRNA
--
ENST00000606573.1FAM66B-2022630No protein-
 
lncRNA
-GENCODE basicTSL:1
ENST00000529456.1FAM66B-2011432No protein-
 
lncRNA
-TSL:2
Statistics

Exons: 6, Coding exons: 0, Transcript length: 2,630 bps,

Transcript Support Level (TSL)

TSL:1

Version

ENST00000606573.1

Type

LncRNA

Annotation Method

Manual annotation (determined on a case-by-case basis) from the Havana project.

GENCODE basic gene

This transcript is a member of the Gencode basic gene set.