Canonical Allele Identifier: CA7648836
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 519231
dbSNP Id: rs369224427

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322697G>A , CM000677.2:g.73322697G>A GRCh38
NC_000015.9:g.73615038G>A , CM000677.1:g.73615038G>A GRCh37
NC_000015.8:g.71402091G>A NCBI36
NG_009063.1:g.51568C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.3396C>T MANE Select ENSP00000261917.3:p.Ser1132=
ENST00000261917.3:c.3396C>T ENSP00000261917.3:p.Ser1132=
NM_005477.2:c.3396C>T NP_005468.1:p.Ser1132=
XM_011521148.1:c.2178C>T XP_011519450.1:p.Ser726=
XM_011521148.2:c.2178C>T XP_011519450.1:p.Ser726=
NM_005477.3:c.3396C>T MANE Select NP_005468.1:p.Ser1132=