Canonical Allele Identifier: CA2187186715

Gene: HCN4

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73322799C= , CM000677.2:g.73322799C=	GRCh38
NC_000015.9:g.73615140C= , CM000677.1:g.73615140C=	GRCh37
NC_000015.8:g.71402193C=	NCBI36
NG_009063.1:g.51466G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.3294G= MANE Select	ENSP00000261917.3:p.Ala1098=
ENST00000261917.3:c.3294G=	ENSP00000261917.3:p.Ala1098=
NM_005477.2:c.3294G=	NP_005468.1:p.Ala1098=
XM_011521148.1:c.2076G=	XP_011519450.1:p.Ala692=
XM_011521148.2:c.2076G=	XP_011519450.1:p.Ala692=
NM_005477.3:c.3294G= MANE Select	NP_005468.1:p.Ala1098=