Canonical Allele Identifier: CA440890582
Gene: FABP2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.120241861G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.119320706G>A , CM000666.2:g.119320706G>A GRCh38
NC_000004.11:g.120241861G>A , CM000666.1:g.120241861G>A GRCh37
NC_000004.10:g.120461309G>A NCBI36
NG_011444.1:g.6456C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000274024.4:c.204C>T MANE Select ENSP00000274024.3:p.Thr68=
ENST00000274024.3:c.204C>T ENSP00000274024.3:p.Thr68=
NM_000134.3:c.204C>T NP_000125.2:p.Thr68=
NM_000134.4:c.204C>T MANE Select NP_000125.2:p.Thr68=