Canonical Allele Identifier: CA2187167395

Gene: HCN4

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73329590G= , CM000677.2:g.73329590G=	GRCh38
NC_000015.9:g.73621931G= , CM000677.1:g.73621931G=	GRCh37
NC_000015.8:g.71408984G=	NCBI36
NG_009063.1:g.44675C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.1573C= MANE Select	ENSP00000261917.3:p.Arg525=
ENST00000261917.3:c.1573C=	ENSP00000261917.3:p.Arg525=
NM_005477.2:c.1573C=	NP_005468.1:p.Arg525=
XM_011521148.1:c.355C=	XP_011519450.1:p.Arg119=
XM_011521148.2:c.355C=	XP_011519450.1:p.Arg119=
NM_005477.3:c.1573C= MANE Select	NP_005468.1:p.Arg525=