Canonical Allele Identifier: CA2187186698

Gene: HCN4

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73322779G= , CM000677.2:g.73322779G=	GRCh38
NC_000015.9:g.73615120G= , CM000677.1:g.73615120G=	GRCh37
NC_000015.8:g.71402173G=	NCBI36
NG_009063.1:g.51486C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.3314C= MANE Select	ENSP00000261917.3:p.Ser1105=
ENST00000261917.3:c.3314C=	ENSP00000261917.3:p.Ser1105=
NM_005477.2:c.3314C=	NP_005468.1:p.Ser1105=
XM_011521148.1:c.2096C=	XP_011519450.1:p.Ser699=
XM_011521148.2:c.2096C=	XP_011519450.1:p.Ser699=
NM_005477.3:c.3314C= MANE Select	NP_005468.1:p.Ser1105=