Canonical Allele Identifier: CA358026886
Gene: FABP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.119320699A>G , CM000666.2:g.119320699A>G GRCh38
NC_000004.11:g.120241854A>G , CM000666.1:g.120241854A>G GRCh37
NC_000004.10:g.120461302A>G NCBI36
NG_011444.1:g.6463T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000274024.4:c.211T>C MANE Select ENSP00000274024.3:p.Tyr71His
ENST00000274024.3:c.211T>C ENSP00000274024.3:p.Tyr71His
NM_000134.3:c.211T>C NP_000125.2:p.Tyr71His
NM_000134.4:c.211T>C MANE Select NP_000125.2:p.Tyr71His