Canonical Allele Identifier: CA491478359

Gene: HCN4

Linked Data

• MyVariant Identifiers: chr15:g.73615383T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73323042T>A , CM000677.2:g.73323042T>A	GRCh38
NC_000015.9:g.73615383T>A , CM000677.1:g.73615383T>A	GRCh37
NC_000015.8:g.71402436T>A	NCBI36
NG_009063.1:g.51223A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.3051A>T MANE Select	ENSP00000261917.3:p.Val1017=
ENST00000261917.3:c.3051A>T	ENSP00000261917.3:p.Val1017=
NM_005477.2:c.3051A>T	NP_005468.1:p.Val1017=
XM_011521148.1:c.1833A>T	XP_011519450.1:p.Val611=
XM_011521148.2:c.1833A>T	XP_011519450.1:p.Val611=
NM_005477.3:c.3051A>T MANE Select	NP_005468.1:p.Val1017=