Canonical Allele Identifier: CA440891372
Gene: FABP2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.120241987T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.119320832T>A , CM000666.2:g.119320832T>A GRCh38
NC_000004.11:g.120241987T>A , CM000666.1:g.120241987T>A GRCh37
NC_000004.10:g.120461435T>A NCBI36
NG_011444.1:g.6330A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000274024.4:c.78A>T MANE Select ENSP00000274024.3:p.Ile26=
ENST00000274024.3:c.78A>T ENSP00000274024.3:p.Ile26=
NM_000134.3:c.78A>T NP_000125.2:p.Ile26=
NM_000134.4:c.78A>T MANE Select NP_000125.2:p.Ile26=
Search 100 bp 5'
Search 100 bp 3'