Canonical Allele Identifier: CA2648170524

Gene: CHRNB2

Linked Data

• gnomAD v4: 1-154571666-G-GTTTTTTA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154571666_154571667insTTTTTTA , CM000663.2:g.154571666_154571667insTTTTTTA	GRCh38
NC_000001.10:g.154544142_154544143insTTTTTTA , CM000663.1:g.154544142_154544143insTTTTTTA	GRCh37
NC_000001.9:g.152810766_152810767insTTTTTTA	NCBI36
NG_008027.1:g.8886_8887insTTTTTTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368476.4:c.843_844insTTTTTTA MANE Select	ENSP00000357461.3:p.Leu282PhefsTer?
ENST00000636034.1:c.843_844insTTTTTTA	ENSP00000489703.1:p.Leu282PhefsTer?
ENST00000637900.1:c.849_850insTTTTTTA	ENSP00000490474.1:p.Leu284PhefsTer?
ENST00000368476.3:c.843_844insTTTTTTA	ENSP00000357461.3:p.Leu282PhefsTer?
NM_000748.2:c.843_844insTTTTTTA	NP_000739.1:p.Leu282PhefsTer?
XM_017000180.2:c.333_334insTTTTTTA	XP_016855669.1:p.Leu112PhefsTer?
XR_001736952.2:n.1095_1096insTTTTTTA
NM_000748.3:c.843_844insTTTTTTA MANE Select	NP_000739.1:p.Leu282PhefsTer?