Canonical Allele Identifier: CA2187167671

Gene: HCN4

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73329759C= , CM000677.2:g.73329759C=	GRCh38
NC_000015.9:g.73622100C= , CM000677.1:g.73622100C=	GRCh37
NC_000015.8:g.71409153C=	NCBI36
NG_009063.1:g.44506G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.1404G= MANE Select	ENSP00000261917.3:p.Ala468=
ENST00000261917.3:c.1404G=	ENSP00000261917.3:p.Ala468=
NM_005477.2:c.1404G=	NP_005468.1:p.Ala468=
XM_011521148.1:c.186G=	XP_011519450.1:p.Ala62=
XM_011521148.2:c.186G=	XP_011519450.1:p.Ala62=
NM_005477.3:c.1404G= MANE Select	NP_005468.1:p.Ala468=