Canonical Allele Identifier: CA2480925376

Gene: CHRNB2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154571782A= , CM000663.2:g.154571782A=	GRCh38
NC_000001.10:g.154544258A= , CM000663.1:g.154544258A=	GRCh37
NC_000001.9:g.152810882A=	NCBI36
NG_008027.1:g.9002A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368476.4:c.959A= MANE Select	ENSP00000357461.3:p.Asn320=
ENST00000636034.1:c.959A=	ENSP00000489703.1:p.Asn320=
ENST00000637900.1:c.965A=	ENSP00000490474.1:p.Asn322=
ENST00000368476.3:c.959A=	ENSP00000357461.3:p.Asn320=
NM_000748.2:c.959A=	NP_000739.1:p.Asn320=
XM_017000180.2:c.449A=	XP_016855669.1:p.Asn150=
XR_001736952.2:n.1211A=
NM_000748.3:c.959A= MANE Select	NP_000739.1:p.Asn320=