Canonical Allele Identifier: CA2187167354

Gene: HCN4

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73329558C= , CM000677.2:g.73329558C=	GRCh38
NC_000015.9:g.73621899C= , CM000677.1:g.73621899C=	GRCh37
NC_000015.8:g.71408952C=	NCBI36
NG_009063.1:g.44707G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261917.4:c.1590+15G= MANE Select	ENSP00000261917.3:n.1590+15G=
ENST00000261917.3:c.1590+15G=	ENSP00000261917.3:n.1590+15G=
NM_005477.2:c.1590+15G=	NP_005468.1:n.1590+15G=
XM_011521148.1:c.372+15G=	XP_011519450.1:n.372+15G=
XM_011521148.2:c.372+15G=	XP_011519450.1:n.372+15G=
NM_005477.3:c.1590+15G= MANE Select	NP_005468.1:n.1590+15G=