Canonical Allele Identifier: CA393085620
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1730220

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322771A>C , CM000677.2:g.73322771A>C GRCh38
NC_000015.9:g.73615112A>C , CM000677.1:g.73615112A>C GRCh37
NC_000015.8:g.71402165A>C NCBI36
NG_009063.1:g.51494T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.3322T>G MANE Select ENSP00000261917.3:p.Ser1108Ala
ENST00000261917.3:c.3322T>G ENSP00000261917.3:p.Ser1108Ala
NM_005477.2:c.3322T>G NP_005468.1:p.Ser1108Ala
XM_011521148.1:c.2104T>G XP_011519450.1:p.Ser702Ala
XM_011521148.2:c.2104T>G XP_011519450.1:p.Ser702Ala
NM_005477.3:c.3322T>G MANE Select NP_005468.1:p.Ser1108Ala