Canonical Allele Identifier: CA358027352
Gene: FABP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.119320764G>A , CM000666.2:g.119320764G>A GRCh38
NC_000004.11:g.120241919G>A , CM000666.1:g.120241919G>A GRCh37
NC_000004.10:g.120461367G>A NCBI36
NG_011444.1:g.6398C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000274024.4:c.146C>T MANE Select ENSP00000274024.3:p.Thr49Ile
ENST00000274024.3:c.146C>T ENSP00000274024.3:p.Thr49Ile
NM_000134.3:c.146C>T NP_000125.2:p.Thr49Ile
NM_000134.4:c.146C>T MANE Select NP_000125.2:p.Thr49Ile