Canonical Allele Identifier: CA2187185897

Gene: HCN4

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73322401A= , CM000677.2:g.73322401A=	GRCh38
NC_000015.9:g.73614742A= , CM000677.1:g.73614742A=	GRCh37
NC_000015.8:g.71401795A=	NCBI36
NG_009063.1:g.51864T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.*80T= MANE Select	ENSP00000261917.3:n.*80T=
ENST00000261917.3:c.*80T=	ENSP00000261917.3:n.*80T=
NM_005477.2:c.*80T=	NP_005468.1:n.*80T=
XM_011521148.1:c.*80T=	XP_011519450.1:n.*80T=
XM_011521148.2:c.*80T=	XP_011519450.1:n.*80T=
NM_005477.3:c.*80T= MANE Select	NP_005468.1:n.*80T=