Canonical Allele Identifier: CA1148722002

Gene: CHRNB2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154571735C= , CM000663.2:g.154571735C=	GRCh38
NC_000001.10:g.154544211C= , CM000663.1:g.154544211C=	GRCh37
NC_000001.9:g.152810835C=	NCBI36
NG_008027.1:g.8955C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368476.4:c.912C= MANE Select	ENSP00000357461.3:p.Thr304=
ENST00000636034.1:c.912C=	ENSP00000489703.1:p.Thr304=
ENST00000637900.1:c.918C=	ENSP00000490474.1:p.Thr306=
ENST00000368476.3:c.912C=	ENSP00000357461.3:p.Thr304=
NM_000748.2:c.912C=	NP_000739.1:p.Thr304=
XM_017000180.2:c.402C=	XP_016855669.1:p.Thr134=
XR_001736952.2:n.1164C=
NM_000748.3:c.912C= MANE Select	NP_000739.1:p.Thr304=