Canonical Allele Identifier: CA2245821766

Gene: CHRNB1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7454194A= , CM000679.2:g.7454194A=	GRCh38
NC_000017.10:g.7357513A= , CM000679.1:g.7357513A=	GRCh37
NC_000017.9:g.7298237A=	NCBI36
NG_008026.1:g.14108A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306071.7:c.821-103A= MANE Select	ENSP00000304290.2:n.821-103A=
ENST00000306071.6:c.821-103A=	ENSP00000304290.2:n.821-103A=
ENST00000536404.6:c.605-103A=	ENSP00000439209.2:n.605-103A=
ENST00000570557.5:c.484-103A=
ENST00000573209.1:n.1765-103A=
ENST00000576360.1:c.605-250A=	ENSP00000459092.1:n.605-250A=
NM_000747.2:c.821-103A=	NP_000738.2:n.821-103A=
NM_000747.3:c.821-103A= MANE Select	NP_000738.2:n.821-103A=