Canonical Allele Identifier: CA2187167477

Gene: HCN4

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73329652G= , CM000677.2:g.73329652G=	GRCh38
NC_000015.9:g.73621993G= , CM000677.1:g.73621993G=	GRCh37
NC_000015.8:g.71409046G=	NCBI36
NG_009063.1:g.44613C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.1511C= MANE Select	ENSP00000261917.3:p.Thr504=
ENST00000261917.3:c.1511C=	ENSP00000261917.3:p.Thr504=
NM_005477.2:c.1511C=	NP_005468.1:p.Thr504=
XM_011521148.1:c.293C=	XP_011519450.1:p.Thr98=
XM_011521148.2:c.293C=	XP_011519450.1:p.Thr98=
NM_005477.3:c.1511C= MANE Select	NP_005468.1:p.Thr504=