Canonical Allele Identifier: CA2187187064

Gene: HCN4

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73322962C= , CM000677.2:g.73322962C=	GRCh38
NC_000015.9:g.73615303C= , CM000677.1:g.73615303C=	GRCh37
NC_000015.8:g.71402356C=	NCBI36
NG_009063.1:g.51303G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.3131G= MANE Select	ENSP00000261917.3:p.Arg1044=
ENST00000261917.3:c.3131G=	ENSP00000261917.3:p.Arg1044=
NM_005477.2:c.3131G=	NP_005468.1:p.Arg1044=
XM_011521148.1:c.1913G=	XP_011519450.1:p.Arg638=
XM_011521148.2:c.1913G=	XP_011519450.1:p.Arg638=
NM_005477.3:c.3131G= MANE Select	NP_005468.1:p.Arg1044=