Canonical Allele Identifier: CA14798772
Gene: HNF4A HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs2144908

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44357077G>A , CM000682.2:g.44357077G>A GRCh38
NC_000020.9:g.42419131G>A NCBI36
NC_000020.10:g.42985717G>A , CM000682.1:g.42985717G>A GRCh37
NG_009818.1:g.6277G>A , LRG_483:g.6277G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000316673.8:c.49+1224G>A ENSP00000315180.4:p.=
ENST00000457232.5:c.49+1224G>A ENSP00000396216.1:p.=
ENST00000609262.5:c.-183+1224G>A ENSP00000476310.1:p.=
ENST00000609795.5:c.49+1224G>A ENSP00000476609.1:p.=
ENST00000619550.4:c.-183+1224G>A ENSP00000481331.1:p.=
NM_001030003.2:c.49+1224G>A NP_001025174.1:p.=
NM_001030004.2:c.49+1224G>A NP_001025175.1:p.=
NM_001287182.1:c.-183+1224G>A NP_001274111.1:p.=
NM_001287183.1:c.-183+1224G>A , LRG_483t3:c.-183+1224G>A NP_001274112.1:p.=
NM_001287184.1:c.-183+1224G>A NP_001274113.1:p.=
NM_175914.4:c.49+1224G>A , LRG_483t1:c.49+1224G>A NP_787110.2:p.=