Canonical Allele Identifier: CA7648881
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 412793
dbSNP Id: rs749785521

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322976C>T , CM000677.2:g.73322976C>T GRCh38
NC_000015.9:g.73615317C>T , CM000677.1:g.73615317C>T GRCh37
NC_000015.8:g.71402370C>T NCBI36
NG_009063.1:g.51289G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.3117G>A MANE Select ENSP00000261917.3:p.Pro1039=
ENST00000261917.3:c.3117G>A ENSP00000261917.3:p.Pro1039=
NM_005477.2:c.3117G>A NP_005468.1:p.Pro1039=
XM_011521148.1:c.1899G>A XP_011519450.1:p.Pro633=
XM_011521148.2:c.1899G>A XP_011519450.1:p.Pro633=
NM_005477.3:c.3117G>A MANE Select NP_005468.1:p.Pro1039=