Canonical Allele Identifier: CA2480925378

Gene: CHRNB2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154571784G= , CM000663.2:g.154571784G=	GRCh38
NC_000001.10:g.154544260G= , CM000663.1:g.154544260G=	GRCh37
NC_000001.9:g.152810884G=	NCBI36
NG_008027.1:g.9004G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368476.4:c.961G= MANE Select	ENSP00000357461.3:p.Val321=
ENST00000636034.1:c.961G=	ENSP00000489703.1:p.Val321=
ENST00000637900.1:c.967G=	ENSP00000490474.1:p.Val323=
ENST00000368476.3:c.961G=	ENSP00000357461.3:p.Val321=
NM_000748.2:c.961G=	NP_000739.1:p.Val321=
XM_017000180.2:c.451G=	XP_016855669.1:p.Val151=
XR_001736952.2:n.1213G=
NM_000748.3:c.961G= MANE Select	NP_000739.1:p.Val321=