Canonical Allele Identifier: CA2245822581

Gene: CHRNB1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7455877G= , CM000679.2:g.7455877G=	GRCh38
NC_000017.10:g.7359196G= , CM000679.1:g.7359196G=	GRCh37
NC_000017.9:g.7299920G=	NCBI36
NG_008026.1:g.15791G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306071.7:c.1301G= MANE Select	ENSP00000304290.2:p.Arg434=
ENST00000306071.6:c.1301G=	ENSP00000304290.2:p.Arg434=
ENST00000536404.6:c.1085G=	ENSP00000439209.2:p.Arg362=
ENST00000575379.1:c.-92G=	ENSP00000461751.1:n.-92G=
ENST00000576360.1:c.938G=	ENSP00000459092.1:p.Arg313=
NM_000747.2:c.1301G=	NP_000738.2:p.Arg434=
NM_000747.3:c.1301G= MANE Select	NP_000738.2:p.Arg434=