Canonical Allele Identifier: CA2187186310

Gene: HCN4

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73322603G= , CM000677.2:g.73322603G=	GRCh38
NC_000015.9:g.73614944G= , CM000677.1:g.73614944G=	GRCh37
NC_000015.8:g.71401997G=	NCBI36
NG_009063.1:g.51662C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.3490C= MANE Select	ENSP00000261917.3:p.Pro1164=
ENST00000261917.3:c.3490C=	ENSP00000261917.3:p.Pro1164=
NM_005477.2:c.3490C=	NP_005468.1:p.Pro1164=
XM_011521148.1:c.2272C=	XP_011519450.1:p.Pro758=
XM_011521148.2:c.2272C=	XP_011519450.1:p.Pro758=
NM_005477.3:c.3490C= MANE Select	NP_005468.1:p.Pro1164=