Canonical Allele Identifier: CA2187187313

Gene: HCN4

Genomic Alleles

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

Transcript Alleles

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