Canonical Allele Identifier: CA2187188651

Gene: HCN4

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73323784G= , CM000677.2:g.73323784G=	GRCh38
NC_000015.9:g.73616125G= , CM000677.1:g.73616125G=	GRCh37
NC_000015.8:g.71403178G=	NCBI36
NG_009063.1:g.50481C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261917.4:c.2309C= MANE Select	ENSP00000261917.3:p.Thr770=
ENST00000261917.3:c.2309C=	ENSP00000261917.3:p.Thr770=
NM_005477.2:c.2309C=	NP_005468.1:p.Thr770=
XM_011521148.1:c.1091C=	XP_011519450.1:p.Thr364=
XM_011521148.2:c.1091C=	XP_011519450.1:p.Thr364=
NM_005477.3:c.2309C= MANE Select	NP_005468.1:p.Thr770=