Canonical Allele Identifier: CA440891002
Gene: FABP2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.120241927A>G (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.119320772A>G , CM000666.2:g.119320772A>G GRCh38
NC_000004.11:g.120241927A>G , CM000666.1:g.120241927A>G GRCh37
NC_000004.10:g.120461375A>G NCBI36
NG_011444.1:g.6390T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000274024.4:c.138T>C MANE Select ENSP00000274024.3:p.Asn46=
ENST00000274024.3:c.138T>C ENSP00000274024.3:p.Asn46=
NM_000134.3:c.138T>C NP_000125.2:p.Asn46=
NM_000134.4:c.138T>C MANE Select NP_000125.2:p.Asn46=
Search 100 bp 5'
Search 100 bp 3'