Canonical Allele Identifier: CA7648817
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 519345
dbSNP Id: rs779811451

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322606G>T , CM000677.2:g.73322606G>T GRCh38
NC_000015.9:g.73614947G>T , CM000677.1:g.73614947G>T GRCh37
NC_000015.8:g.71402000G>T NCBI36
NG_009063.1:g.51659C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.3487C>A MANE Select ENSP00000261917.3:p.Pro1163Thr
ENST00000261917.3:c.3487C>A ENSP00000261917.3:p.Pro1163Thr
NM_005477.2:c.3487C>A NP_005468.1:p.Pro1163Thr
XM_011521148.1:c.2269C>A XP_011519450.1:p.Pro757Thr
XM_011521148.2:c.2269C>A XP_011519450.1:p.Pro757Thr
NM_005477.3:c.3487C>A MANE Select NP_005468.1:p.Pro1163Thr