Canonical Allele Identifier: CA2187186591

Gene: HCN4

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73322728G= , CM000677.2:g.73322728G=	GRCh38
NC_000015.9:g.73615069G= , CM000677.1:g.73615069G=	GRCh37
NC_000015.8:g.71402122G=	NCBI36
NG_009063.1:g.51537C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.3365C= MANE Select	ENSP00000261917.3:p.Ala1122=
ENST00000261917.3:c.3365C=	ENSP00000261917.3:p.Ala1122=
NM_005477.2:c.3365C=	NP_005468.1:p.Ala1122=
XM_011521148.1:c.2147C=	XP_011519450.1:p.Ala716=
XM_011521148.2:c.2147C=	XP_011519450.1:p.Ala716=
NM_005477.3:c.3365C= MANE Select	NP_005468.1:p.Ala1122=