Canonical Allele Identifier: CA2187187070

Gene: HCN4

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73322963G= , CM000677.2:g.73322963G=	GRCh38
NC_000015.9:g.73615304G= , CM000677.1:g.73615304G=	GRCh37
NC_000015.8:g.71402357G=	NCBI36
NG_009063.1:g.51302C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.3130C= MANE Select	ENSP00000261917.3:p.Arg1044=
ENST00000261917.3:c.3130C=	ENSP00000261917.3:p.Arg1044=
NM_005477.2:c.3130C=	NP_005468.1:p.Arg1044=
XM_011521148.1:c.1912C=	XP_011519450.1:p.Arg638=
XM_011521148.2:c.1912C=	XP_011519450.1:p.Arg638=
NM_005477.3:c.3130C= MANE Select	NP_005468.1:p.Arg1044=