Canonical Allele Identifier: CA2187188205

Gene: HCN4

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73323396T= , CM000677.2:g.73323396T=	GRCh38
NC_000015.9:g.73615737T= , CM000677.1:g.73615737T=	GRCh37
NC_000015.8:g.71402790T=	NCBI36
NG_009063.1:g.50869A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261917.4:c.2697A= MANE Select	ENSP00000261917.3:p.Val899=
ENST00000261917.3:c.2697A=	ENSP00000261917.3:p.Val899=
NM_005477.2:c.2697A=	NP_005468.1:p.Val899=
XM_011521148.1:c.1479A=	XP_011519450.1:p.Val493=
XM_011521148.2:c.1479A=	XP_011519450.1:p.Val493=
NM_005477.3:c.2697A= MANE Select	NP_005468.1:p.Val899=