Canonical Allele Identifier: CA15979146
Gene: HNF4A HGNC NCBI
HNF4A-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs4812829
gnomAD v2: 20-42989267-G-A
gnomAD v3: 20-44360627-G-A
gnomAD v4: 20-44360627-G-A
MyVariant Identifiers: chr20:g.42989267G>A (hg19) chr20:g.44360627G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44360627G>A , CM000682.2:g.44360627G>A GRCh38
NC_000020.10:g.42989267G>A , CM000682.1:g.42989267G>A GRCh37
NC_000020.9:g.42422681G>A NCBI36
NG_009818.1:g.9827G>A , LRG_483:g.9827G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000316673.9:c.49+4774G>A (HNF4A) MANE Select ENSP00000315180.4:n.49+4774G>A
ENST00000316673.8:c.49+4774G>A (HNF4A) ENSP00000315180.4:n.49+4774G>A
ENST00000457232.5:c.49+4774G>A (HNF4A) ENSP00000396216.1:n.49+4774G>A
ENST00000609262.5:c.-183+4774G>A (HNF4A) ENSP00000476310.1:n.-183+4774G>A
ENST00000609795.5:c.49+4774G>A (HNF4A) ENSP00000476609.1:n.49+4774G>A
ENST00000619550.4:c.-183+4774G>A (HNF4A) ENSP00000481331.1:n.-183+4774G>A
NM_001030003.2:c.49+4774G>A (HNF4A) NP_001025174.1:n.49+4774G>A
NM_001030004.2:c.49+4774G>A (HNF4A) NP_001025175.1:n.49+4774G>A
NM_001287182.1:c.-183+4774G>A (HNF4A) NP_001274111.1:n.-183+4774G>A
NM_001287183.1:c.-183+4774G>A , LRG_483t3:c.-183+4774G>A (HNF4A) NP_001274112.1:n.-183+4774G>A
NM_001287184.1:c.-183+4774G>A (HNF4A) NP_001274113.1:n.-183+4774G>A
NM_175914.4:c.49+4774G>A , LRG_483t1:c.49+4774G>A (HNF4A) NP_787110.2:n.49+4774G>A
NM_001030003.3:c.49+4774G>A (HNF4A) NP_001025174.1:n.49+4774G>A
NM_001030004.3:c.49+4774G>A (HNF4A) NP_001025175.1:n.49+4774G>A
NM_001287182.2:c.-183+4774G>A (HNF4A) NP_001274111.1:n.-183+4774G>A
NM_001287184.2:c.-183+4774G>A (HNF4A) NP_001274113.1:n.-183+4774G>A
NM_001287183.2:c.-183+4774G>A (HNF4A) NP_001274112.1:n.-183+4774G>A
NM_175914.5:c.49+4774G>A (HNF4A) MANE Select NP_787110.2:n.49+4774G>A
NR_172878.1:n.655C>T (HNF4A-AS1)
Search 100 bp 5'
Search 100 bp 3'