Canonical Allele Identifier: CA2187186915

Gene: HCN4

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73322893T= , CM000677.2:g.73322893T=	GRCh38
NC_000015.9:g.73615234T= , CM000677.1:g.73615234T=	GRCh37
NC_000015.8:g.71402287T=	NCBI36
NG_009063.1:g.51372A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.3200A= MANE Select	ENSP00000261917.3:p.Gln1067=
ENST00000261917.3:c.3200A=	ENSP00000261917.3:p.Gln1067=
NM_005477.2:c.3200A=	NP_005468.1:p.Gln1067=
XM_011521148.1:c.1982A=	XP_011519450.1:p.Gln661=
XM_011521148.2:c.1982A=	XP_011519450.1:p.Gln661=
NM_005477.3:c.3200A= MANE Select	NP_005468.1:p.Gln1067=