Canonical Allele Identifier: CA2187186570

Gene: HCN4

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73322721A= , CM000677.2:g.73322721A=	GRCh38
NC_000015.9:g.73615062A= , CM000677.1:g.73615062A=	GRCh37
NC_000015.8:g.71402115A=	NCBI36
NG_009063.1:g.51544T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.3372T= MANE Select	ENSP00000261917.3:p.Gly1124=
ENST00000261917.3:c.3372T=	ENSP00000261917.3:p.Gly1124=
NM_005477.2:c.3372T=	NP_005468.1:p.Gly1124=
XM_011521148.1:c.2154T=	XP_011519450.1:p.Gly718=
XM_011521148.2:c.2154T=	XP_011519450.1:p.Gly718=
NM_005477.3:c.3372T= MANE Select	NP_005468.1:p.Gly1124=