Canonical Allele Identifier: CA393097856
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 660308
ClinVar RCV Id: RCV000817474 RCV002478906
dbSNP Id: rs1489387068
gnomAD v2: 15-73660119-G-A
gnomAD v4: 15-73367778-G-A
MyVariant Identifiers: chr15:g.73660119G>A (hg19) chr15:g.73367778G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73367778G>A , CM000677.2:g.73367778G>A GRCh38
NC_000015.9:g.73660119G>A , CM000677.1:g.73660119G>A GRCh37
NC_000015.8:g.71447172G>A NCBI36
NG_009063.1:g.6487C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.493C>T MANE Select ENSP00000261917.3:p.Pro165Ser
ENST00000261917.3:c.493C>T ENSP00000261917.3:p.Pro165Ser
NM_005477.2:c.493C>T NP_005468.1:p.Pro165Ser
NM_005477.3:c.493C>T MANE Select NP_005468.1:p.Pro165Ser
Search 100 bp 5'
Search 100 bp 3'