Canonical Allele Identifier: CA2480925366

Gene: CHRNB2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154571749_154571752delinsCCTT , CM000663.2:g.154571749_154571752delinsCCTT	GRCh38
NC_000001.10:g.154544225_154544228delinsCCTT , CM000663.1:g.154544225_154544228delinsCCTT	GRCh37
NC_000001.9:g.152810849_152810852delinsCCTT	NCBI36
NG_008027.1:g.8969_8972delinsCCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368476.4:c.926_929delinsCCTT MANE Select	ENSP00000357461.3:p.Thr309=
ENST00000636034.1:c.926_929delinsCCTT	ENSP00000489703.1:p.Thr309=
ENST00000637900.1:c.932_935delinsCCTT	ENSP00000490474.1:p.Thr311=
ENST00000368476.3:c.926_929delinsCCTT	ENSP00000357461.3:p.Thr309=
NM_000748.2:c.926_929delinsCCTT	NP_000739.1:p.Thr309=
XM_017000180.2:c.416_419delinsCCTT	XP_016855669.1:p.Thr139=
XR_001736952.2:n.1178_1181delinsCCTT
NM_000748.3:c.926_929delinsCCTT MANE Select	NP_000739.1:p.Thr309=