Canonical Allele Identifier: CA2480925369

Gene: CHRNB2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154571753C= , CM000663.2:g.154571753C=	GRCh38
NC_000001.10:g.154544229C= , CM000663.1:g.154544229C=	GRCh37
NC_000001.9:g.152810853C=	NCBI36
NG_008027.1:g.8973C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368476.4:c.930C= MANE Select	ENSP00000357461.3:p.Phe310=
ENST00000636034.1:c.930C=	ENSP00000489703.1:p.Phe310=
ENST00000637900.1:c.936C=	ENSP00000490474.1:p.Phe312=
ENST00000368476.3:c.930C=	ENSP00000357461.3:p.Phe310=
NM_000748.2:c.930C=	NP_000739.1:p.Phe310=
XM_017000180.2:c.420C=	XP_016855669.1:p.Phe140=
XR_001736952.2:n.1182C=
NM_000748.3:c.930C= MANE Select	NP_000739.1:p.Phe310=