Canonical Allele Identifier: CA491479277
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2988757
ClinVar RCV Id: RCV003846924
MyVariant Identifiers: chr15:g.73660174T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73367833T>A , CM000677.2:g.73367833T>A GRCh38
NC_000015.9:g.73660174T>A , CM000677.1:g.73660174T>A GRCh37
NC_000015.8:g.71447227T>A NCBI36
NG_009063.1:g.6432A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.438A>T MANE Select ENSP00000261917.3:p.Pro146=
ENST00000261917.3:c.438A>T ENSP00000261917.3:p.Pro146=
NM_005477.2:c.438A>T NP_005468.1:p.Pro146=
NM_005477.3:c.438A>T MANE Select NP_005468.1:p.Pro146=
Search 100 bp 5'
Search 100 bp 3'