Canonical Allele Identifier: CA2746189170

Gene: CHRNB2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154571686_154571687insACCCCCACACCAAACAC , CM000663.2:g.154571686_154571687insACCCCCACACCAAACAC	GRCh38
NC_000001.10:g.154544162_154544163insACCCCCACACCAAACAC , CM000663.1:g.154544162_154544163insACCCCCACACCAAACAC	GRCh37
NC_000001.9:g.152810786_152810787insACCCCCACACCAAACAC	NCBI36
NG_008027.1:g.8906_8907insACCCCCACACCAAACAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368476.4:c.863_864insACCCCCACACCAAACAC MANE Select	ENSP00000357461.3:p.Thr290ProfsTer?
ENST00000636034.1:c.863_864insACCCCCACACCAAACAC	ENSP00000489703.1:p.Thr290ProfsTer?
ENST00000637900.1:c.869_870insACCCCCACACCAAACAC	ENSP00000490474.1:p.Thr292ProfsTer?
ENST00000368476.3:c.863_864insACCCCCACACCAAACAC	ENSP00000357461.3:p.Thr290ProfsTer?
NM_000748.2:c.863_864insACCCCCACACCAAACAC	NP_000739.1:p.Thr290ProfsTer?
XM_017000180.2:c.353_354insACCCCCACACCAAACAC	XP_016855669.1:p.Thr120ProfsTer?
XR_001736952.2:n.1115_1116insACCCCCACACCAAACAC
NM_000748.3:c.863_864insACCCCCACACCAAACAC MANE Select	NP_000739.1:p.Thr290ProfsTer?