Canonical Allele Identifier: CA393086385

Gene: HCN4

Linked Data

• gnomAD v4: 15-73323061-G-A
• MyVariant Identifiers: chr15:g.73615402G>A (hg19) ; chr15:g.73323061G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73323061G>A , CM000677.2:g.73323061G>A	GRCh38
NC_000015.9:g.73615402G>A , CM000677.1:g.73615402G>A	GRCh37
NC_000015.8:g.71402455G>A	NCBI36
NG_009063.1:g.51204C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.3032C>T MANE Select	ENSP00000261917.3:p.Ser1011Phe
ENST00000261917.3:c.3032C>T	ENSP00000261917.3:p.Ser1011Phe
NM_005477.2:c.3032C>T	NP_005468.1:p.Ser1011Phe
XM_011521148.1:c.1814C>T	XP_011519450.1:p.Ser605Phe
XM_011521148.2:c.1814C>T	XP_011519450.1:p.Ser605Phe
NM_005477.3:c.3032C>T MANE Select	NP_005468.1:p.Ser1011Phe