Canonical Allele Identifier: CA358027623
Gene: FABP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.119320789T>G , CM000666.2:g.119320789T>G GRCh38
NC_000004.11:g.120241944T>G , CM000666.1:g.120241944T>G GRCh37
NC_000004.10:g.120461392T>G NCBI36
NG_011444.1:g.6373A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000274024.4:c.121A>C MANE Select ENSP00000274024.3:p.Ile41Leu
ENST00000274024.3:c.121A>C ENSP00000274024.3:p.Ile41Leu
NM_000134.3:c.121A>C NP_000125.2:p.Ile41Leu
NM_000134.4:c.121A>C MANE Select NP_000125.2:p.Ile41Leu