Canonical Allele Identifier: CA2187188773

Gene: HCN4

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73323895A= , CM000677.2:g.73323895A=	GRCh38
NC_000015.9:g.73616236A= , CM000677.1:g.73616236A=	GRCh37
NC_000015.8:g.71403289A=	NCBI36
NG_009063.1:g.50370T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261917.4:c.2198T= MANE Select	ENSP00000261917.3:p.Val733=
ENST00000261917.3:c.2198T=	ENSP00000261917.3:p.Val733=
NM_005477.2:c.2198T=	NP_005468.1:p.Val733=
XM_011521148.1:c.980T=	XP_011519450.1:p.Val327=
XM_011521148.2:c.980T=	XP_011519450.1:p.Val327=
NM_005477.3:c.2198T= MANE Select	NP_005468.1:p.Val733=