Canonical Allele Identifier: CA2480925232

Gene: CHRNB2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154571366_154571367delinsAG , CM000663.2:g.154571366_154571367delinsAG	GRCh38
NC_000001.10:g.154543842_154543843delinsAG , CM000663.1:g.154543842_154543843delinsAG	GRCh37
NC_000001.9:g.152810466_152810467delinsAG	NCBI36
NG_008027.1:g.8586_8587delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368476.4:c.543_544delinsAG MANE Select	ENSP00000357461.3:p.Thr181=
ENST00000636034.1:c.543_544delinsAG	ENSP00000489703.1:p.Thr181=
ENST00000637900.1:c.549_550delinsAG	ENSP00000490474.1:p.Thr183=
ENST00000368476.3:c.543_544delinsAG	ENSP00000357461.3:p.Thr181=
NM_000748.2:c.543_544delinsAG	NP_000739.1:p.Thr181=
XM_017000180.2:c.33_34delinsAG	XP_016855669.1:p.Thr11=
XR_001736952.2:n.795_796delinsAG
NM_000748.3:c.543_544delinsAG MANE Select	NP_000739.1:p.Thr181=