Canonical Allele Identifier: CA2245822292

Gene: CHRNB1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7455353G= , CM000679.2:g.7455353G=	GRCh38
NC_000017.10:g.7358672G= , CM000679.1:g.7358672G=	GRCh37
NC_000017.9:g.7299396G=	NCBI36
NG_008026.1:g.15267G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000306071.7:c.1114G= MANE Select	ENSP00000304290.2:p.Glu372=
ENST00000306071.6:c.1114G=	ENSP00000304290.2:p.Glu372=
ENST00000536404.6:c.898G=	ENSP00000439209.2:p.Glu300=
ENST00000570557.5:c.777G=
ENST00000573209.1:n.2058G=
ENST00000576360.1:c.751G=	ENSP00000459092.1:p.Glu251=
NM_000747.2:c.1114G=	NP_000738.2:p.Glu372=
NM_000747.3:c.1114G= MANE Select	NP_000738.2:p.Glu372=