Canonical Allele Identifier: CA7648853
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 470665
dbSNP Id: rs753734843

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322804C>T , CM000677.2:g.73322804C>T GRCh38
NC_000015.9:g.73615145C>T , CM000677.1:g.73615145C>T GRCh37
NC_000015.8:g.71402198C>T NCBI36
NG_009063.1:g.51461G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.3289G>A MANE Select ENSP00000261917.3:p.Gly1097Arg
ENST00000261917.3:c.3289G>A ENSP00000261917.3:p.Gly1097Arg
NM_005477.2:c.3289G>A NP_005468.1:p.Gly1097Arg
XM_011521148.1:c.2071G>A XP_011519450.1:p.Gly691Arg
XM_011521148.2:c.2071G>A XP_011519450.1:p.Gly691Arg
NM_005477.3:c.3289G>A MANE Select NP_005468.1:p.Gly1097Arg