Canonical Allele Identifier: CA1143652181

Gene: CHRNB2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154571252C= , CM000663.2:g.154571252C=	GRCh38
NC_000001.10:g.154543728C= , CM000663.1:g.154543728C=	GRCh37
NC_000001.9:g.152810352C=	NCBI36
NG_008027.1:g.8472C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368476.4:c.429C= MANE Select	ENSP00000357461.3:p.Ile143=
ENST00000636034.1:c.429C=	ENSP00000489703.1:p.Ile143=
ENST00000637900.1:c.435C=	ENSP00000490474.1:p.Ile145=
ENST00000368476.3:c.429C=	ENSP00000357461.3:p.Ile143=
NM_000748.2:c.429C=	NP_000739.1:p.Ile143=
XM_017000180.2:c.-9-73C=	XP_016855669.1:n.-9-73C=
XR_001736952.2:n.681C=
NM_000748.3:c.429C= MANE Select	NP_000739.1:p.Ile143=