Canonical Allele Identifier: CA393098473
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2883676
ClinVar RCV Id: RCV003615118
dbSNP Id: rs1230290081
gnomAD v2: 15-73660323-G-A
gnomAD v4: 15-73367982-G-A
MyVariant Identifiers: chr15:g.73660323G>A (hg19) chr15:g.73367982G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73367982G>A , CM000677.2:g.73367982G>A GRCh38
NC_000015.9:g.73660323G>A , CM000677.1:g.73660323G>A GRCh37
NC_000015.8:g.71447376G>A NCBI36
NG_009063.1:g.6283C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.289C>T MANE Select ENSP00000261917.3:p.Arg97Cys
ENST00000261917.3:c.289C>T ENSP00000261917.3:p.Arg97Cys
NM_005477.2:c.289C>T NP_005468.1:p.Arg97Cys
NM_005477.3:c.289C>T MANE Select NP_005468.1:p.Arg97Cys
Search 100 bp 5'
Search 100 bp 3'