Canonical Allele Identifier: CA2480925354

Gene: CHRNB2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154571714C= , CM000663.2:g.154571714C=	GRCh38
NC_000001.10:g.154544190C= , CM000663.1:g.154544190C=	GRCh37
NC_000001.9:g.152810814C=	NCBI36
NG_008027.1:g.8934C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368476.4:c.891C= MANE Select	ENSP00000357461.3:p.Val297=
ENST00000636034.1:c.891C=	ENSP00000489703.1:p.Val297=
ENST00000637900.1:c.897C=	ENSP00000490474.1:p.Val299=
ENST00000368476.3:c.891C=	ENSP00000357461.3:p.Val297=
NM_000748.2:c.891C=	NP_000739.1:p.Val297=
XM_017000180.2:c.381C=	XP_016855669.1:p.Val127=
XR_001736952.2:n.1143C=
NM_000748.3:c.891C= MANE Select	NP_000739.1:p.Val297=