Canonical Allele Identifier: CA2245821836

Gene: CHRNB1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7454345T= , CM000679.2:g.7454345T=	GRCh38
NC_000017.10:g.7357664T= , CM000679.1:g.7357664T=	GRCh37
NC_000017.9:g.7298388T=	NCBI36
NG_008026.1:g.14259T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306071.7:c.869T= MANE Select	ENSP00000304290.2:p.Phe290=
ENST00000306071.6:c.869T=	ENSP00000304290.2:p.Phe290=
ENST00000536404.6:c.653T=	ENSP00000439209.2:p.Phe218=
ENST00000570557.5:c.532T=
ENST00000573209.1:n.1813T=
ENST00000576360.1:c.605-99T=	ENSP00000459092.1:n.605-99T=
NM_000747.2:c.869T=	NP_000738.2:p.Phe290=
NM_000747.3:c.869T= MANE Select	NP_000738.2:p.Phe290=