Canonical Allele Identifier: CA1143478801

Gene: CHRNB2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154571751T= , CM000663.2:g.154571751T=	GRCh38
NC_000001.10:g.154544227T= , CM000663.1:g.154544227T=	GRCh37
NC_000001.9:g.152810851T=	NCBI36
NG_008027.1:g.8971T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368476.4:c.928T= MANE Select	ENSP00000357461.3:p.Phe310=
ENST00000636034.1:c.928T=	ENSP00000489703.1:p.Phe310=
ENST00000637900.1:c.934T=	ENSP00000490474.1:p.Phe312=
ENST00000368476.3:c.928T=	ENSP00000357461.3:p.Phe310=
NM_000748.2:c.928T=	NP_000739.1:p.Phe310=
XM_017000180.2:c.418T=	XP_016855669.1:p.Phe140=
XR_001736952.2:n.1180T=
NM_000748.3:c.928T= MANE Select	NP_000739.1:p.Phe310=