Canonical Allele Identifier: CA2187167905

Gene: HCN4

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73330046C= , CM000677.2:g.73330046C=	GRCh38
NC_000015.9:g.73622387C= , CM000677.1:g.73622387C=	GRCh37
NC_000015.8:g.71409440C=	NCBI36
NG_009063.1:g.44219G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.1372-255G= MANE Select	ENSP00000261917.3:n.1372-255G=
ENST00000261917.3:c.1372-255G=	ENSP00000261917.3:n.1372-255G=
NM_005477.2:c.1372-255G=	NP_005468.1:n.1372-255G=
XM_011521148.1:c.154-255G=	XP_011519450.1:n.154-255G=
XM_011521148.2:c.154-255G=	XP_011519450.1:n.154-255G=
NM_005477.3:c.1372-255G= MANE Select	NP_005468.1:n.1372-255G=