Canonical Allele Identifier: CA16606777
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 382812
dbSNP Id: rs1057521459

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322967C>T , CM000677.2:g.73322967C>T GRCh38
NC_000015.9:g.73615308C>T , CM000677.1:g.73615308C>T GRCh37
NC_000015.8:g.71402361C>T NCBI36
NG_009063.1:g.51298G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.3126G>A MANE Select ENSP00000261917.3:p.Pro1042=
ENST00000261917.3:c.3126G>A ENSP00000261917.3:p.Pro1042=
NM_005477.2:c.3126G>A NP_005468.1:p.Pro1042=
XM_011521148.1:c.1908G>A XP_011519450.1:p.Pro636=
XM_011521148.2:c.1908G>A XP_011519450.1:p.Pro636=
NM_005477.3:c.3126G>A MANE Select NP_005468.1:p.Pro1042=