Canonical Allele Identifier: CA1140796279

Gene: CHRNB2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154569474C= , CM000663.2:g.154569474C=	GRCh38
NC_000001.10:g.154541950C= , CM000663.1:g.154541950C=	GRCh37
NC_000001.9:g.152808574C=	NCBI36
NG_008027.1:g.6694C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000368476.4:c.77C= MANE Select	ENSP00000357461.3:p.Thr26=
ENST00000636034.1:c.77C=	ENSP00000489703.1:p.Thr26=
ENST00000637900.1:c.77C=	ENSP00000490474.1:p.Thr26=
ENST00000368476.3:c.77C=	ENSP00000357461.3:p.Thr26=
NM_000748.2:c.77C=	NP_000739.1:p.Thr26=
XM_017000180.2:c.-298C=	XP_016855669.1:n.-298C=
XR_001736952.2:n.329C=
NM_000748.3:c.77C= MANE Select	NP_000739.1:p.Thr26=