Canonical Allele Identifier: CA2187185966

Gene: HCN4

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73322454G= , CM000677.2:g.73322454G=	GRCh38
NC_000015.9:g.73614795G= , CM000677.1:g.73614795G=	GRCh37
NC_000015.8:g.71401848G=	NCBI36
NG_009063.1:g.51811C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.*27C= MANE Select	ENSP00000261917.3:n.*27C=
ENST00000261917.3:c.*27C=	ENSP00000261917.3:n.*27C=
NM_005477.2:c.*27C=	NP_005468.1:n.*27C=
XM_011521148.1:c.*27C=	XP_011519450.1:n.*27C=
XM_011521148.2:c.*27C=	XP_011519450.1:n.*27C=
NM_005477.3:c.*27C= MANE Select	NP_005468.1:n.*27C=