Canonical Allele Identifier: CA7648952

Gene: HCN4

Linked Data

• ClinVar Variation Id: 470659
• ClinVar RCV Id: RCV000546891
• dbSNP Id: rs775803239
• ExAC: 15:73615630 G / T
• gnomAD v2: 15-73615630-G-T
• gnomAD v3: 15-73323289-G-T
• gnomAD v4: 15-73323289-G-T
• MyVariant Identifiers: chr15:g.73615630G>T (hg19) ; chr15:g.73323289G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73323289G>T , CM000677.2:g.73323289G>T	GRCh38
NC_000015.9:g.73615630G>T , CM000677.1:g.73615630G>T	GRCh37
NC_000015.8:g.71402683G>T	NCBI36
NG_009063.1:g.50976C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000261917.4:c.2804C>A MANE Select	ENSP00000261917.3:p.Ser935Tyr
ENST00000261917.3:c.2804C>A	ENSP00000261917.3:p.Ser935Tyr
NM_005477.2:c.2804C>A	NP_005468.1:p.Ser935Tyr
XM_011521148.1:c.1586C>A	XP_011519450.1:p.Ser529Tyr
XM_011521148.2:c.1586C>A	XP_011519450.1:p.Ser529Tyr
NM_005477.3:c.2804C>A MANE Select	NP_005468.1:p.Ser935Tyr