Canonical Allele Identifier: CA1141927483

Gene: CHRNB2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154569475G= , CM000663.2:g.154569475G=	GRCh38
NC_000001.10:g.154541951G= , CM000663.1:g.154541951G=	GRCh37
NC_000001.9:g.152808575G=	NCBI36
NG_008027.1:g.6695G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000368476.4:c.78G= MANE Select	ENSP00000357461.3:p.Thr26=
ENST00000636034.1:c.78G=	ENSP00000489703.1:p.Thr26=
ENST00000637900.1:c.78G=	ENSP00000490474.1:p.Thr26=
ENST00000368476.3:c.78G=	ENSP00000357461.3:p.Thr26=
NM_000748.2:c.78G=	NP_000739.1:p.Thr26=
XM_017000180.2:c.-297G=	XP_016855669.1:n.-297G=
XR_001736952.2:n.330G=
NM_000748.3:c.78G= MANE Select	NP_000739.1:p.Thr26=