Canonical Allele Identifier: CA2480925349

Gene: CHRNB2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154571708G= , CM000663.2:g.154571708G=	GRCh38
NC_000001.10:g.154544184G= , CM000663.1:g.154544184G=	GRCh37
NC_000001.9:g.152810808G=	NCBI36
NG_008027.1:g.8928G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368476.4:c.885G= MANE Select	ENSP00000357461.3:p.Pro295=
ENST00000636034.1:c.885G=	ENSP00000489703.1:p.Pro295=
ENST00000637900.1:c.891G=	ENSP00000490474.1:p.Pro297=
ENST00000368476.3:c.885G=	ENSP00000357461.3:p.Pro295=
NM_000748.2:c.885G=	NP_000739.1:p.Pro295=
XM_017000180.2:c.375G=	XP_016855669.1:p.Pro125=
XR_001736952.2:n.1137G=
NM_000748.3:c.885G= MANE Select	NP_000739.1:p.Pro295=