Canonical Allele Identifier: CA090974
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 432269
dbSNP Id: rs200395062

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323673C>T , CM000677.2:g.73323673C>T GRCh38
NC_000015.9:g.73616014C>T , CM000677.1:g.73616014C>T GRCh37
NC_000015.8:g.71403067C>T NCBI36
NG_009063.1:g.50592G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.2420G>A MANE Select ENSP00000261917.3:p.Arg807His
ENST00000261917.3:c.2420G>A ENSP00000261917.3:p.Arg807His
NM_005477.2:c.2420G>A NP_005468.1:p.Arg807His
XM_011521148.1:c.1202G>A XP_011519450.1:p.Arg401His
XM_011521148.2:c.1202G>A XP_011519450.1:p.Arg401His
NM_005477.3:c.2420G>A MANE Select NP_005468.1:p.Arg807His