Canonical Allele Identifier: CA2480925360

Gene: CHRNB2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154571733A= , CM000663.2:g.154571733A=	GRCh38
NC_000001.10:g.154544209A= , CM000663.1:g.154544209A=	GRCh37
NC_000001.9:g.152810833A=	NCBI36
NG_008027.1:g.8953A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368476.4:c.910A= MANE Select	ENSP00000357461.3:p.Thr304=
ENST00000636034.1:c.910A=	ENSP00000489703.1:p.Thr304=
ENST00000637900.1:c.916A=	ENSP00000490474.1:p.Thr306=
ENST00000368476.3:c.910A=	ENSP00000357461.3:p.Thr304=
NM_000748.2:c.910A=	NP_000739.1:p.Thr304=
XM_017000180.2:c.400A=	XP_016855669.1:p.Thr134=
XR_001736952.2:n.1162A=
NM_000748.3:c.910A= MANE Select	NP_000739.1:p.Thr304=