Canonical Allele Identifier: CA2733120164
Gene: CHRNB1 HGNC NCBI

Linked Data

dbSNP Id: rs2150843264

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7455774del , CM000679.2:g.7455774del GRCh38
NC_000017.10:g.7359093del , CM000679.1:g.7359093del GRCh37
NC_000017.9:g.7299817del NCBI36
NG_008026.1:g.15688del

Transcript Alleles

HGVS Amino-acid change
ENST00000306071.7:c.1218-20del MANE Select ENSP00000304290.2:n.1218-20del
ENST00000306071.6:c.1218-20del ENSP00000304290.2:n.1218-20del
ENST00000536404.6:c.1002-20del ENSP00000439209.2:n.1002-20del
ENST00000570557.5:c.881-20del
ENST00000575379.1:c.-195del ENSP00000461751.1:n.-195del
ENST00000576360.1:c.855-20del ENSP00000459092.1:n.855-20del
NM_000747.2:c.1218-20del NP_000738.2:n.1218-20del
NM_000747.3:c.1218-20del MANE Select NP_000738.2:n.1218-20del