Canonical Allele Identifier: CA2648170690

Gene: CHRNB2

Linked Data

• gnomAD v4: 1-154571708-G-GTATT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154571708_154571709insTATT , CM000663.2:g.154571708_154571709insTATT	GRCh38
NC_000001.10:g.154544184_154544185insTATT , CM000663.1:g.154544184_154544185insTATT	GRCh37
NC_000001.9:g.152810808_152810809insTATT	NCBI36
NG_008027.1:g.8928_8929insTATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368476.4:c.885_886insTATT MANE Select	ENSP00000357461.3:p.Leu296TyrfsTer?
ENST00000636034.1:c.885_886insTATT	ENSP00000489703.1:p.Leu296TyrfsTer?
ENST00000637900.1:c.891_892insTATT	ENSP00000490474.1:p.Leu298TyrfsTer?
ENST00000368476.3:c.885_886insTATT	ENSP00000357461.3:p.Leu296TyrfsTer?
NM_000748.2:c.885_886insTATT	NP_000739.1:p.Leu296TyrfsTer?
XM_017000180.2:c.375_376insTATT	XP_016855669.1:p.Leu126TyrfsTer?
XR_001736952.2:n.1137_1138insTATT
NM_000748.3:c.885_886insTATT MANE Select	NP_000739.1:p.Leu296TyrfsTer?