Canonical Allele Identifier: CA2187186324

Gene: HCN4

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73322627T= , CM000677.2:g.73322627T=	GRCh38
NC_000015.9:g.73614968T= , CM000677.1:g.73614968T=	GRCh37
NC_000015.8:g.71402021T=	NCBI36
NG_009063.1:g.51638A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.3466A= MANE Select	ENSP00000261917.3:p.Thr1156=
ENST00000261917.3:c.3466A=	ENSP00000261917.3:p.Thr1156=
NM_005477.2:c.3466A=	NP_005468.1:p.Thr1156=
XM_011521148.1:c.2248A=	XP_011519450.1:p.Thr750=
XM_011521148.2:c.2248A=	XP_011519450.1:p.Thr750=
NM_005477.3:c.3466A= MANE Select	NP_005468.1:p.Thr1156=