Canonical Allele Identifier: CA2245821929

Gene: CHRNB1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7454555_7454556delinsCT , CM000679.2:g.7454555_7454556delinsCT	GRCh38
NC_000017.10:g.7357874_7357875delinsCT , CM000679.1:g.7357874_7357875delinsCT	GRCh37
NC_000017.9:g.7298598_7298599delinsCT	NCBI36
NG_008026.1:g.14469_14470delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306071.7:c.1044+35_1044+36delinsCT MANE Select	ENSP00000304290.2:n.1044+35_1044+36delinsCT
ENST00000306071.6:c.1044+35_1044+36delinsCT	ENSP00000304290.2:n.1044+35_1044+36delinsCT
ENST00000536404.6:c.828+35_828+36delinsCT	ENSP00000439209.2:n.828+35_828+36delinsCT
ENST00000570557.5:c.707+35_707+36delinsCT
ENST00000573209.1:n.1988+35_1988+36delinsCT
ENST00000576360.1:c.681+35_681+36delinsCT	ENSP00000459092.1:n.681+35_681+36delinsCT
NM_000747.2:c.1044+35_1044+36delinsCT	NP_000738.2:n.1044+35_1044+36delinsCT
NM_000747.3:c.1044+35_1044+36delinsCT MANE Select	NP_000738.2:n.1044+35_1044+36delinsCT