Canonical Allele Identifier: CA1148732805

Gene: CHRNB2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154571189T= , CM000663.2:g.154571189T=	GRCh38
NC_000001.10:g.154543665T= , CM000663.1:g.154543665T=	GRCh37
NC_000001.9:g.152810289T=	NCBI36
NG_008027.1:g.8409T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368476.4:c.366T= MANE Select	ENSP00000357461.3:p.Asn122=
ENST00000636034.1:c.366T=	ENSP00000489703.1:p.Asn122=
ENST00000637900.1:c.372T=	ENSP00000490474.1:p.Asn124=
ENST00000368476.3:c.366T=	ENSP00000357461.3:p.Asn122=
NM_000748.2:c.366T=	NP_000739.1:p.Asn122=
XM_017000180.2:c.-9-136T=	XP_016855669.1:n.-9-136T=
XR_001736952.2:n.618T=
NM_000748.3:c.366T= MANE Select	NP_000739.1:p.Asn122=