Canonical Allele Identifier: CA2187186933

Gene: HCN4

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73322899A= , CM000677.2:g.73322899A=	GRCh38
NC_000015.9:g.73615240A= , CM000677.1:g.73615240A=	GRCh37
NC_000015.8:g.71402293A=	NCBI36
NG_009063.1:g.51366T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.3194T= MANE Select	ENSP00000261917.3:p.Val1065=
ENST00000261917.3:c.3194T=	ENSP00000261917.3:p.Val1065=
NM_005477.2:c.3194T=	NP_005468.1:p.Val1065=
XM_011521148.1:c.1976T=	XP_011519450.1:p.Val659=
XM_011521148.2:c.1976T=	XP_011519450.1:p.Val659=
NM_005477.3:c.3194T= MANE Select	NP_005468.1:p.Val1065=