Canonical Allele Identifier: CA2187188649

Gene: HCN4

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73323783C= , CM000677.2:g.73323783C=	GRCh38
NC_000015.9:g.73616124C= , CM000677.1:g.73616124C=	GRCh37
NC_000015.8:g.71403177C=	NCBI36
NG_009063.1:g.50482G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261917.4:c.2310G= MANE Select	ENSP00000261917.3:p.Thr770=
ENST00000261917.3:c.2310G=	ENSP00000261917.3:p.Thr770=
NM_005477.2:c.2310G=	NP_005468.1:p.Thr770=
XM_011521148.1:c.1092G=	XP_011519450.1:p.Thr364=
XM_011521148.2:c.1092G=	XP_011519450.1:p.Thr364=
NM_005477.3:c.2310G= MANE Select	NP_005468.1:p.Thr770=