Canonical Allele Identifier: CA440890698
Gene: FABP2 HGNC NCBI

Linked Data

dbSNP Id: rs1755653066
MyVariant Identifiers: chr4:g.120241882A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.119320727A>C , CM000666.2:g.119320727A>C GRCh38
NC_000004.11:g.120241882A>C , CM000666.1:g.120241882A>C GRCh37
NC_000004.10:g.120461330A>C NCBI36
NG_011444.1:g.6435T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000274024.4:c.183T>G MANE Select ENSP00000274024.3:p.Val61=
ENST00000274024.3:c.183T>G ENSP00000274024.3:p.Val61=
NM_000134.3:c.183T>G NP_000125.2:p.Val61=
NM_000134.4:c.183T>G MANE Select NP_000125.2:p.Val61=