Canonical Allele Identifier: CA2187188455

Gene: HCN4

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73323513T= , CM000677.2:g.73323513T=	GRCh38
NC_000015.9:g.73615854T= , CM000677.1:g.73615854T=	GRCh37
NC_000015.8:g.71402907T=	NCBI36
NG_009063.1:g.50752A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.2580A= MANE Select	ENSP00000261917.3:p.Gln860=
ENST00000261917.3:c.2580A=	ENSP00000261917.3:p.Gln860=
NM_005477.2:c.2580A=	NP_005468.1:p.Gln860=
XM_011521148.1:c.1362A=	XP_011519450.1:p.Gln454=
XM_011521148.2:c.1362A=	XP_011519450.1:p.Gln454=
NM_005477.3:c.2580A= MANE Select	NP_005468.1:p.Gln860=