Canonical Allele Identifier: CA2245821852

Gene: CHRNB1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7454378C= , CM000679.2:g.7454378C=	GRCh38
NC_000017.10:g.7357697C= , CM000679.1:g.7357697C=	GRCh37
NC_000017.9:g.7298421C=	NCBI36
NG_008026.1:g.14292C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306071.7:c.902C= MANE Select	ENSP00000304290.2:p.Thr301=
ENST00000306071.6:c.902C=	ENSP00000304290.2:p.Thr301=
ENST00000536404.6:c.686C=	ENSP00000439209.2:p.Thr229=
ENST00000570557.5:c.565C=
ENST00000573209.1:n.1846C=
ENST00000576360.1:c.605-66C=	ENSP00000459092.1:n.605-66C=
NM_000747.2:c.902C=	NP_000738.2:p.Thr301=
NM_000747.3:c.902C= MANE Select	NP_000738.2:p.Thr301=