Canonical Allele Identifier: CA440890831
Gene: FABP2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.120241906T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.119320751T>A , CM000666.2:g.119320751T>A GRCh38
NC_000004.11:g.120241906T>A , CM000666.1:g.120241906T>A GRCh37
NC_000004.10:g.120461354T>A NCBI36
NG_011444.1:g.6411A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000274024.4:c.159A>T MANE Select ENSP00000274024.3:p.Ser53=
ENST00000274024.3:c.159A>T ENSP00000274024.3:p.Ser53=
NM_000134.3:c.159A>T NP_000125.2:p.Ser53=
NM_000134.4:c.159A>T MANE Select NP_000125.2:p.Ser53=