Canonical Allele Identifier: CA7649467

Gene: HCN4

Linked Data

• ClinVar Variation Id: 942085
• ClinVar RCV Id: RCV001211997 ; RCV003294024 ; RCV004538455
• dbSNP Id: rs753829397
• ExAC: 15:73660075 G / A
• gnomAD v2: 15-73660075-G-A
• gnomAD v3: 15-73367734-G-A
• gnomAD v4: 15-73367734-G-A
• MyVariant Identifiers: chr15:g.73660075G>A (hg19) ; chr15:g.73367734G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73367734G>A , CM000677.2:g.73367734G>A	GRCh38
NC_000015.9:g.73660075G>A , CM000677.1:g.73660075G>A	GRCh37
NC_000015.8:g.71447128G>A	NCBI36
NG_009063.1:g.6531C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.537C>T MANE Select	ENSP00000261917.3:p.Cys179=
ENST00000261917.3:c.537C>T	ENSP00000261917.3:p.Cys179=
NM_005477.2:c.537C>T	NP_005468.1:p.Cys179=
NM_005477.3:c.537C>T MANE Select	NP_005468.1:p.Cys179=