Canonical Allele Identifier: CA2245821866

Gene: CHRNB1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7454423T= , CM000679.2:g.7454423T=	GRCh38
NC_000017.10:g.7357742T= , CM000679.1:g.7357742T=	GRCh37
NC_000017.9:g.7298466T=	NCBI36
NG_008026.1:g.14337T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306071.7:c.947T= MANE Select	ENSP00000304290.2:p.Met316=
ENST00000306071.6:c.947T=	ENSP00000304290.2:p.Met316=
ENST00000536404.6:c.731T=	ENSP00000439209.2:p.Met244=
ENST00000570557.5:c.610T=
ENST00000573209.1:n.1891T=
ENST00000576360.1:c.605-21T=	ENSP00000459092.1:n.605-21T=
NM_000747.2:c.947T=	NP_000738.2:p.Met316=
NM_000747.3:c.947T= MANE Select	NP_000738.2:p.Met316=