Canonical Allele Identifier: CA2480925275

Gene: CHRNB2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154571496A= , CM000663.2:g.154571496A=	GRCh38
NC_000001.10:g.154543972A= , CM000663.1:g.154543972A=	GRCh37
NC_000001.9:g.152810596A=	NCBI36
NG_008027.1:g.8716A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368476.4:c.673A= MANE Select	ENSP00000357461.3:p.Thr225=
ENST00000636034.1:c.673A=	ENSP00000489703.1:p.Thr225=
ENST00000637900.1:c.679A=	ENSP00000490474.1:p.Thr227=
ENST00000368476.3:c.673A=	ENSP00000357461.3:p.Thr225=
NM_000748.2:c.673A=	NP_000739.1:p.Thr225=
XM_017000180.2:c.163A=	XP_016855669.1:p.Thr55=
XR_001736952.2:n.925A=
NM_000748.3:c.673A= MANE Select	NP_000739.1:p.Thr225=