Canonical Allele Identifier: CA3059774
Gene: FABP2 HGNC NCBI

Linked Data

dbSNP Id: rs749763336

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.119320679A>G , CM000666.2:g.119320679A>G GRCh38
NC_000004.11:g.120241834A>G , CM000666.1:g.120241834A>G GRCh37
NC_000004.10:g.120461282A>G NCBI36
NG_011444.1:g.6483T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000274024.4:c.231T>C MANE Select ENSP00000274024.3:p.Thr77=
ENST00000274024.3:c.231T>C ENSP00000274024.3:p.Thr77=
NM_000134.3:c.231T>C NP_000125.2:p.Thr77=
NM_000134.4:c.231T>C MANE Select NP_000125.2:p.Thr77=