Canonical Allele Identifier: CA491478501
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2115939
ClinVar RCV Id: RCV003024468
gnomAD v4: 15-73323402-A-C
MyVariant Identifiers: chr15:g.73615743A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323402A>C , CM000677.2:g.73323402A>C GRCh38
NC_000015.9:g.73615743A>C , CM000677.1:g.73615743A>C GRCh37
NC_000015.8:g.71402796A>C NCBI36
NG_009063.1:g.50863T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.2691T>G MANE Select ENSP00000261917.3:p.Ala897=
ENST00000261917.3:c.2691T>G ENSP00000261917.3:p.Ala897=
NM_005477.2:c.2691T>G NP_005468.1:p.Ala897=
XM_011521148.1:c.1473T>G XP_011519450.1:p.Ala491=
XM_011521148.2:c.1473T>G XP_011519450.1:p.Ala491=
NM_005477.3:c.2691T>G MANE Select NP_005468.1:p.Ala897=
Search 100 bp 5'
Search 100 bp 3'