Canonical Allele Identifier: CA2187188496

Gene: HCN4

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73323542T= , CM000677.2:g.73323542T=	GRCh38
NC_000015.9:g.73615883T= , CM000677.1:g.73615883T=	GRCh37
NC_000015.8:g.71402936T=	NCBI36
NG_009063.1:g.50723A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.2551A= MANE Select	ENSP00000261917.3:p.Thr851=
ENST00000261917.3:c.2551A=	ENSP00000261917.3:p.Thr851=
NM_005477.2:c.2551A=	NP_005468.1:p.Thr851=
XM_011521148.1:c.1333A=	XP_011519450.1:p.Thr445=
XM_011521148.2:c.1333A=	XP_011519450.1:p.Thr445=
NM_005477.3:c.2551A= MANE Select	NP_005468.1:p.Thr851=