Canonical Allele Identifier: CA2187186678

Gene: HCN4

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73322770G= , CM000677.2:g.73322770G=	GRCh38
NC_000015.9:g.73615111G= , CM000677.1:g.73615111G=	GRCh37
NC_000015.8:g.71402164G=	NCBI36
NG_009063.1:g.51495C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.3323C= MANE Select	ENSP00000261917.3:p.Ser1108=
ENST00000261917.3:c.3323C=	ENSP00000261917.3:p.Ser1108=
NM_005477.2:c.3323C=	NP_005468.1:p.Ser1108=
XM_011521148.1:c.2105C=	XP_011519450.1:p.Ser702=
XM_011521148.2:c.2105C=	XP_011519450.1:p.Ser702=
NM_005477.3:c.3323C= MANE Select	NP_005468.1:p.Ser1108=