Canonical Allele Identifier: CA2187186903

Gene: HCN4

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73322890C= , CM000677.2:g.73322890C=	GRCh38
NC_000015.9:g.73615231C= , CM000677.1:g.73615231C=	GRCh37
NC_000015.8:g.71402284C=	NCBI36
NG_009063.1:g.51375G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.3203G= MANE Select	ENSP00000261917.3:p.Arg1068=
ENST00000261917.3:c.3203G=	ENSP00000261917.3:p.Arg1068=
NM_005477.2:c.3203G=	NP_005468.1:p.Arg1068=
XM_011521148.1:c.1985G=	XP_011519450.1:p.Arg662=
XM_011521148.2:c.1985G=	XP_011519450.1:p.Arg662=
NM_005477.3:c.3203G= MANE Select	NP_005468.1:p.Arg1068=