Canonical Allele Identifier: CA2480925351

Gene: CHRNB2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154571711C= , CM000663.2:g.154571711C=	GRCh38
NC_000001.10:g.154544187C= , CM000663.1:g.154544187C=	GRCh37
NC_000001.9:g.152810811C=	NCBI36
NG_008027.1:g.8931C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368476.4:c.888C= MANE Select	ENSP00000357461.3:p.Leu296=
ENST00000636034.1:c.888C=	ENSP00000489703.1:p.Leu296=
ENST00000637900.1:c.894C=	ENSP00000490474.1:p.Leu298=
ENST00000368476.3:c.888C=	ENSP00000357461.3:p.Leu296=
NM_000748.2:c.888C=	NP_000739.1:p.Leu296=
XM_017000180.2:c.378C=	XP_016855669.1:p.Leu126=
XR_001736952.2:n.1140C=
NM_000748.3:c.888C= MANE Select	NP_000739.1:p.Leu296=