Canonical Allele Identifier: CA1143378285

Gene: CHRNB2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154571220T= , CM000663.2:g.154571220T=	GRCh38
NC_000001.10:g.154543696T= , CM000663.1:g.154543696T=	GRCh37
NC_000001.9:g.152810320T=	NCBI36
NG_008027.1:g.8440T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368476.4:c.397T= MANE Select	ENSP00000357461.3:p.Ser133=
ENST00000636034.1:c.397T=	ENSP00000489703.1:p.Ser133=
ENST00000637900.1:c.403T=	ENSP00000490474.1:p.Ser135=
ENST00000368476.3:c.397T=	ENSP00000357461.3:p.Ser133=
NM_000748.2:c.397T=	NP_000739.1:p.Ser133=
XM_017000180.2:c.-9-105T=	XP_016855669.1:n.-9-105T=
XR_001736952.2:n.649T=
NM_000748.3:c.397T= MANE Select	NP_000739.1:p.Ser133=