Canonical Allele Identifier: CA393085007
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2738232
ClinVar RCV Id: RCV003506626

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322567C>A , CM000677.2:g.73322567C>A GRCh38
NC_000015.9:g.73614908C>A , CM000677.1:g.73614908C>A GRCh37
NC_000015.8:g.71401961C>A NCBI36
NG_009063.1:g.51698G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.3526G>T MANE Select ENSP00000261917.3:p.Gly1176Trp
ENST00000261917.3:c.3526G>T ENSP00000261917.3:p.Gly1176Trp
NM_005477.2:c.3526G>T NP_005468.1:p.Gly1176Trp
XM_011521148.1:c.2308G>T XP_011519450.1:p.Gly770Trp
XM_011521148.2:c.2308G>T XP_011519450.1:p.Gly770Trp
NM_005477.3:c.3526G>T MANE Select NP_005468.1:p.Gly1176Trp