Canonical Allele Identifier: CA2187188547

Gene: HCN4

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73323579G= , CM000677.2:g.73323579G=	GRCh38
NC_000015.9:g.73615920G= , CM000677.1:g.73615920G=	GRCh37
NC_000015.8:g.71402973G=	NCBI36
NG_009063.1:g.50686C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.2514C= MANE Select	ENSP00000261917.3:p.Gly838=
ENST00000261917.3:c.2514C=	ENSP00000261917.3:p.Gly838=
NM_005477.2:c.2514C=	NP_005468.1:p.Gly838=
XM_011521148.1:c.1296C=	XP_011519450.1:p.Gly432=
XM_011521148.2:c.1296C=	XP_011519450.1:p.Gly432=
NM_005477.3:c.2514C= MANE Select	NP_005468.1:p.Gly838=