Canonical Allele Identifier: CA2187167629

Gene: HCN4

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73329724C= , CM000677.2:g.73329724C=	GRCh38
NC_000015.9:g.73622065C= , CM000677.1:g.73622065C=	GRCh37
NC_000015.8:g.71409118C=	NCBI36
NG_009063.1:g.44541G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.1439G= MANE Select	ENSP00000261917.3:p.Gly480=
ENST00000261917.3:c.1439G=	ENSP00000261917.3:p.Gly480=
NM_005477.2:c.1439G=	NP_005468.1:p.Gly480=
XM_011521148.1:c.221G=	XP_011519450.1:p.Gly74=
XM_011521148.2:c.221G=	XP_011519450.1:p.Gly74=
NM_005477.3:c.1439G= MANE Select	NP_005468.1:p.Gly480=