Canonical Allele Identifier: CA2187187229

Gene: HCN4

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73323015G= , CM000677.2:g.73323015G=	GRCh38
NC_000015.9:g.73615356G= , CM000677.1:g.73615356G=	GRCh37
NC_000015.8:g.71402409G=	NCBI36
NG_009063.1:g.51250C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.3078C= MANE Select	ENSP00000261917.3:p.Ser1026=
ENST00000261917.3:c.3078C=	ENSP00000261917.3:p.Ser1026=
NM_005477.2:c.3078C=	NP_005468.1:p.Ser1026=
XM_011521148.1:c.1860C=	XP_011519450.1:p.Ser620=
XM_011521148.2:c.1860C=	XP_011519450.1:p.Ser620=
NM_005477.3:c.3078C= MANE Select	NP_005468.1:p.Ser1026=