Canonical Allele Identifier: CA104693317

Gene: FABP2

Linked Data

• dbSNP Id: rs528675853
• gnomAD v3: 4-119320493-A-G
• gnomAD v4: 4-119320493-A-G
• MyVariant Identifiers: chr4:g.120241648A>G (hg19) ; chr4:g.119320493A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.119320493A>G , CM000666.2:g.119320493A>G	GRCh38
NC_000004.11:g.120241648A>G , CM000666.1:g.120241648A>G	GRCh37
NC_000004.10:g.120461096A>G	NCBI36
NG_011444.1:g.6669T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274024.4:c.240+177T>C MANE Select	ENSP00000274024.3:n.240+177T>C
ENST00000274024.3:c.240+177T>C	ENSP00000274024.3:n.240+177T>C
NM_000134.3:c.240+177T>C	NP_000125.2:n.240+177T>C
NM_000134.4:c.240+177T>C MANE Select	NP_000125.2:n.240+177T>C