Canonical Allele Identifier: CA393088566

Gene: HCN4

Linked Data

• gnomAD v4: 15-73323490-G-T
• MyVariant Identifiers: chr15:g.73615831G>T (hg19) ; chr15:g.73323490G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73323490G>T , CM000677.2:g.73323490G>T	GRCh38
NC_000015.9:g.73615831G>T , CM000677.1:g.73615831G>T	GRCh37
NC_000015.8:g.71402884G>T	NCBI36
NG_009063.1:g.50775C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.2603C>A MANE Select	ENSP00000261917.3:p.Pro868His
ENST00000261917.3:c.2603C>A	ENSP00000261917.3:p.Pro868His
NM_005477.2:c.2603C>A	NP_005468.1:p.Pro868His
XM_011521148.1:c.1385C>A	XP_011519450.1:p.Pro462His
XM_011521148.2:c.1385C>A	XP_011519450.1:p.Pro462His
NM_005477.3:c.2603C>A MANE Select	NP_005468.1:p.Pro868His