Canonical Allele Identifier: CA1488878463
Gene: FABP2 HGNC NCBI

Linked Data

dbSNP Id: rs1578611988

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.119320551C>T , CM000666.2:g.119320551C>T GRCh38
NC_000004.11:g.120241706C>T , CM000666.1:g.120241706C>T GRCh37
NC_000004.10:g.120461154C>T NCBI36
NG_011444.1:g.6611G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000274024.4:c.240+119G>A MANE Select ENSP00000274024.3:n.240+119G>A
ENST00000274024.3:c.240+119G>A ENSP00000274024.3:n.240+119G>A
NM_000134.3:c.240+119G>A NP_000125.2:n.240+119G>A
NM_000134.4:c.240+119G>A MANE Select NP_000125.2:n.240+119G>A