Canonical Allele Identifier: CA2245821973

Gene: CHRNB1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7454681C= , CM000679.2:g.7454681C=	GRCh38
NC_000017.10:g.7358000C= , CM000679.1:g.7358000C=	GRCh37
NC_000017.9:g.7298724C=	NCBI36
NG_008026.1:g.14595C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306071.7:c.1044+161C= MANE Select	ENSP00000304290.2:n.1044+161C=
ENST00000306071.6:c.1044+161C=	ENSP00000304290.2:n.1044+161C=
ENST00000536404.6:c.828+161C=	ENSP00000439209.2:n.828+161C=
ENST00000570557.5:c.707+161C=
ENST00000573209.1:n.1988+161C=
ENST00000576360.1:c.681+161C=	ENSP00000459092.1:n.681+161C=
NM_000747.2:c.1044+161C=	NP_000738.2:n.1044+161C=
NM_000747.3:c.1044+161C= MANE Select	NP_000738.2:n.1044+161C=