Canonical Allele Identifier: CA2245821874

Gene: CHRNB1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7454435C= , CM000679.2:g.7454435C=	GRCh38
NC_000017.10:g.7357754C= , CM000679.1:g.7357754C=	GRCh37
NC_000017.9:g.7298478C=	NCBI36
NG_008026.1:g.14349C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306071.7:c.959C= MANE Select	ENSP00000304290.2:p.Thr320=
ENST00000306071.6:c.959C=	ENSP00000304290.2:p.Thr320=
ENST00000536404.6:c.743C=	ENSP00000439209.2:p.Thr248=
ENST00000570557.5:c.622C=
ENST00000573209.1:n.1903C=
ENST00000576360.1:c.605-9C=	ENSP00000459092.1:n.605-9C=
NM_000747.2:c.959C=	NP_000738.2:p.Thr320=
NM_000747.3:c.959C= MANE Select	NP_000738.2:p.Thr320=