Canonical Allele Identifier: CA2187188368

Gene: HCN4

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73323474T= , CM000677.2:g.73323474T=	GRCh38
NC_000015.9:g.73615815T= , CM000677.1:g.73615815T=	GRCh37
NC_000015.8:g.71402868T=	NCBI36
NG_009063.1:g.50791A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.2619A= MANE Select	ENSP00000261917.3:p.Pro873=
ENST00000261917.3:c.2619A=	ENSP00000261917.3:p.Pro873=
NM_005477.2:c.2619A=	NP_005468.1:p.Pro873=
XM_011521148.1:c.1401A=	XP_011519450.1:p.Pro467=
XM_011521148.2:c.1401A=	XP_011519450.1:p.Pro467=
NM_005477.3:c.2619A= MANE Select	NP_005468.1:p.Pro873=