Canonical Allele Identifier: CA358027711
Gene: FABP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.119320801A>T , CM000666.2:g.119320801A>T GRCh38
NC_000004.11:g.120241956A>T , CM000666.1:g.120241956A>T GRCh37
NC_000004.10:g.120461404A>T NCBI36
NG_011444.1:g.6361T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000274024.4:c.109T>A MANE Select ENSP00000274024.3:p.Leu37Met
ENST00000274024.3:c.109T>A ENSP00000274024.3:p.Leu37Met
NM_000134.3:c.109T>A NP_000125.2:p.Leu37Met
NM_000134.4:c.109T>A MANE Select NP_000125.2:p.Leu37Met