Canonical Allele Identifier: CA2746189169

Gene: CHRNB2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154571685_154571686insA , CM000663.2:g.154571685_154571686insA	GRCh38
NC_000001.10:g.154544161_154544162insA , CM000663.1:g.154544161_154544162insA	GRCh37
NC_000001.9:g.152810785_152810786insA	NCBI36
NG_008027.1:g.8905_8906insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368476.4:c.862_863insA MANE Select	ENSP00000357461.3:p.Pro288HisfsTer?
ENST00000636034.1:c.862_863insA	ENSP00000489703.1:p.Pro288HisfsTer?
ENST00000637900.1:c.868_869insA	ENSP00000490474.1:p.Pro290HisfsTer?
ENST00000368476.3:c.862_863insA	ENSP00000357461.3:p.Pro288HisfsTer?
NM_000748.2:c.862_863insA	NP_000739.1:p.Pro288HisfsTer?
XM_017000180.2:c.352_353insA	XP_016855669.1:p.Pro118HisfsTer?
XR_001736952.2:n.1114_1115insA
NM_000748.3:c.862_863insA MANE Select	NP_000739.1:p.Pro288HisfsTer?