Canonical Allele Identifier: CA7649405

Gene: HCN4

Linked Data

• ClinVar Variation Id: 2195171
• ClinVar RCV Id: RCV002647605
• dbSNP Id: rs781732180
• ExAC: 15:73636159 G / A
• gnomAD v2: 15-73636159-G-A
• gnomAD v3: 15-73343818-G-A
• gnomAD v4: 15-73343818-G-A
• MyVariant Identifiers: chr15:g.73636159G>A (hg19) ; chr15:g.73343818G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73343818G>A , CM000677.2:g.73343818G>A	GRCh38
NC_000015.9:g.73636159G>A , CM000677.1:g.73636159G>A	GRCh37
NC_000015.8:g.71423212G>A	NCBI36
NG_009063.1:g.30447C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.786-10C>T MANE Select	ENSP00000261917.3:n.786-10C>T
ENST00000261917.3:c.786-10C>T	ENSP00000261917.3:n.786-10C>T
NM_005477.2:c.786-10C>T	NP_005468.1:n.786-10C>T
NM_005477.3:c.786-10C>T MANE Select	NP_005468.1:n.786-10C>T