Canonical Allele Identifier: CA2480927318

Gene: CHRNB2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154576206G= , CM000663.2:g.154576206G=	GRCh38
NC_000001.10:g.154548682G= , CM000663.1:g.154548682G=	GRCh37
NC_000001.9:g.152815306G=	NCBI36
NG_008027.1:g.13426G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368476.4:c.*274G= MANE Select	ENSP00000357461.3:n.*274G=
ENST00000636034.1:c.1505+278G=	ENSP00000489703.1:n.1505+278G=
ENST00000637900.1:c.*274G=	ENSP00000490474.1:n.*274G=
ENST00000368476.3:c.*274G=	ENSP00000357461.3:n.*274G=
NM_000748.2:c.*274G=	NP_000739.1:n.*274G=
XM_017000180.2:c.*274G=	XP_016855669.1:n.*274G=
XR_001736952.2:n.2035G=
NM_000748.3:c.*274G= MANE Select	NP_000739.1:n.*274G=