Human (GRCh38.p14)
Description

FSHD region gene 2 family member C [Source:HGNC Symbol;Acc:HGNC:33626]

Location

Chromosome 3: 75,664,328-75,667,220 forward strand.

GRCh38:CM000665.2

About this gene

This gene has 2 transcripts (splice variants), 58 orthologues and 2 paralogues.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000308062.8FRG2C-2012033282aaENSP00000312299.3
 
Protein coding
CCDS43108A6NGY1 NM_001124759.5MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P2TSL:1
ENST00000464571.1FRG2C-2022075281aaENSP00000419432.1
 
Protein coding
CCDS93313C9JUX3 -GENCODE basicAPPRIS ALT2TSL:1