Canonical Allele Identifier: CA393097448
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1752212
ClinVar RCV Id: RCV002366470

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73367651C>A , CM000677.2:g.73367651C>A GRCh38
NC_000015.9:g.73659992C>A , CM000677.1:g.73659992C>A GRCh37
NC_000015.8:g.71447045C>A NCBI36
NG_009063.1:g.6614G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.620G>T MANE Select ENSP00000261917.3:p.Arg207Leu
ENST00000261917.3:c.620G>T ENSP00000261917.3:p.Arg207Leu
NM_005477.2:c.620G>T NP_005468.1:p.Arg207Leu
NM_005477.3:c.620G>T MANE Select NP_005468.1:p.Arg207Leu