Canonical Allele Identifier: CA14757881
Gene: HNF4A HGNC NCBI
HNF4A-AS1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs2425637

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44395409G>T , CM000682.2:g.44395409G>T GRCh38
NC_000020.10:g.43024049G>T , CM000682.1:g.43024049G>T GRCh37
NC_000020.9:g.42457463G>T NCBI36
NG_009818.1:g.44609G>T , LRG_483:g.44609G>T

Transcript Alleles

HGVS Amino-acid change
NM_001030003.2:c.50-10649G>T (HNF4A) VV NP_001025174.1:p.=
NM_001030004.2:c.50-10649G>T (HNF4A) VV NP_001025175.1:p.=
NM_001287182.1:c.40+4730G>T (HNF4A) VV NP_001274111.1:p.=
NM_001287183.1:c.40+4730G>T , LRG_483t3:c.40+4730G>T (HNF4A) NP_001274112.1:p.=
NM_001287184.1:c.40+4730G>T (HNF4A) VV NP_001274113.1:p.=
NM_175914.4:c.50-10649G>T , LRG_483t1:c.50-10649G>T (HNF4A) NP_787110.2:p.=
NR_109949.1:n.254+44C>A (HNF4A-AS1)
ENST00000316673.8:c.50-10649G>T ENSP00000315180.4:p.=
ENST00000457232.5:c.50-10649G>T ENSP00000396216.1:p.=
ENST00000609262.5:c.40+4730G>T ENSP00000476310.1:p.=
ENST00000609795.5:c.50-10649G>T ENSP00000476609.1:p.=
ENST00000619550.4:c.40+4730G>T ENSP00000481331.1:p.=