Canonical Allele Identifier: CA7648853

Gene: HCN4

Linked Data

• ClinVar Variation Id: 470665
• ClinVar RCV Id: RCV000548525 ; RCV002476178 ; RCV002448742
• dbSNP Id: rs753734843
• ExAC: 15:73615145 C / T
• gnomAD v2: 15-73615145-C-T
• gnomAD v3: 15-73322804-C-T
• gnomAD v4: 15-73322804-C-T
• MyVariant Identifiers: chr15:g.73615145C>T (hg19) ; chr15:g.73322804C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73322804C>T , CM000677.2:g.73322804C>T	GRCh38
NC_000015.9:g.73615145C>T , CM000677.1:g.73615145C>T	GRCh37
NC_000015.8:g.71402198C>T	NCBI36
NG_009063.1:g.51461G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.3289G>A MANE Select	ENSP00000261917.3:p.Gly1097Arg
ENST00000261917.3:c.3289G>A	ENSP00000261917.3:p.Gly1097Arg
NM_005477.2:c.3289G>A	NP_005468.1:p.Gly1097Arg
XM_011521148.1:c.2071G>A	XP_011519450.1:p.Gly691Arg
XM_011521148.2:c.2071G>A	XP_011519450.1:p.Gly691Arg
NM_005477.3:c.3289G>A MANE Select	NP_005468.1:p.Gly1097Arg