Canonical Allele Identifier: CA393085389
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 470669
ClinVar RCV Id: RCV000539007
dbSNP Id: rs1377027284

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322686C>A , CM000677.2:g.73322686C>A GRCh38
NC_000015.9:g.73615027C>A , CM000677.1:g.73615027C>A GRCh37
NC_000015.8:g.71402080C>A NCBI36
NG_009063.1:g.51579G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.3407G>T MANE Select ENSP00000261917.3:p.Gly1136Val
ENST00000261917.3:c.3407G>T ENSP00000261917.3:p.Gly1136Val
NM_005477.2:c.3407G>T NP_005468.1:p.Gly1136Val
XM_011521148.1:c.2189G>T XP_011519450.1:p.Gly730Val
XM_011521148.2:c.2189G>T XP_011519450.1:p.Gly730Val
NM_005477.3:c.3407G>T MANE Select NP_005468.1:p.Gly1136Val