Canonical Allele Identifier: CA358027848
Gene: FABP2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.120241977T>A (hg19) chr4:g.119320822T>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.119320822T>A , CM000666.2:g.119320822T>A GRCh38
NC_000004.11:g.120241977T>A , CM000666.1:g.120241977T>A GRCh37
NC_000004.10:g.120461425T>A NCBI36
NG_011444.1:g.6340A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000274024.4:c.88A>T MANE Select ENSP00000274024.3:p.Lys30Ter
ENST00000274024.3:c.88A>T ENSP00000274024.3:p.Lys30Ter
NM_000134.3:c.88A>T NP_000125.2:p.Lys30Ter
NM_000134.4:c.88A>T MANE Select NP_000125.2:p.Lys30Ter
Search 100 bp 5'
Search 100 bp 3'