Canonical Allele Identifier: CA2187169761

Gene: HCN4

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73332164A= , CM000677.2:g.73332164A=	GRCh38
NC_000015.9:g.73624505A= , CM000677.1:g.73624505A=	GRCh37
NC_000015.8:g.71411558A=	NCBI36
NG_009063.1:g.42101T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261917.4:c.1338T= MANE Select	ENSP00000261917.3:p.Pro446=
ENST00000261917.3:c.1338T=	ENSP00000261917.3:p.Pro446=
NM_005477.2:c.1338T=	NP_005468.1:p.Pro446=
XM_011521148.1:c.120T=	XP_011519450.1:p.Pro40=
XM_011521148.2:c.120T=	XP_011519450.1:p.Pro40=
NM_005477.3:c.1338T= MANE Select	NP_005468.1:p.Pro446=