Canonical Allele Identifier: CA2187188426

Gene: HCN4

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73323498G= , CM000677.2:g.73323498G=	GRCh38
NC_000015.9:g.73615839G= , CM000677.1:g.73615839G=	GRCh37
NC_000015.8:g.71402892G=	NCBI36
NG_009063.1:g.50767C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.2595C= MANE Select	ENSP00000261917.3:p.Phe865=
ENST00000261917.3:c.2595C=	ENSP00000261917.3:p.Phe865=
NM_005477.2:c.2595C=	NP_005468.1:p.Phe865=
XM_011521148.1:c.1377C=	XP_011519450.1:p.Phe459=
XM_011521148.2:c.1377C=	XP_011519450.1:p.Phe459=
NM_005477.3:c.2595C= MANE Select	NP_005468.1:p.Phe865=