Canonical Allele Identifier: CA2671895155

Gene: FABP2

Linked Data

• gnomAD v4: 4-119320901-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.119320901T>C , CM000666.2:g.119320901T>C	GRCh38
NC_000004.11:g.120242056T>C , CM000666.1:g.120242056T>C	GRCh37
NC_000004.10:g.120461504T>C	NCBI36
NG_011444.1:g.6261A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274024.4:c.68-59A>G MANE Select	ENSP00000274024.3:n.68-59A>G
ENST00000274024.3:c.68-59A>G	ENSP00000274024.3:n.68-59A>G
NM_000134.3:c.68-59A>G	NP_000125.2:n.68-59A>G
NM_000134.4:c.68-59A>G MANE Select	NP_000125.2:n.68-59A>G