Canonical Allele Identifier: CA2245822533
Gene: CHRNB1 HGNC NCBI

Linked Data

dbSNP Id: rs2069943649

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7455785del , CM000679.2:g.7455785del GRCh38
NC_000017.10:g.7359104del , CM000679.1:g.7359104del GRCh37
NC_000017.9:g.7299828del NCBI36
NG_008026.1:g.15699del

Transcript Alleles

HGVS Amino-acid change
ENST00000306071.7:c.1218-9del MANE Select ENSP00000304290.2:n.1218-9del
ENST00000306071.6:c.1218-9del ENSP00000304290.2:n.1218-9del
ENST00000536404.6:c.1002-9del ENSP00000439209.2:n.1002-9del
ENST00000570557.5:c.881-9del
ENST00000575379.1:c.-184del ENSP00000461751.1:n.-184del
ENST00000576360.1:c.855-9del ENSP00000459092.1:n.855-9del
NM_000747.2:c.1218-9del NP_000738.2:n.1218-9del
NM_000747.3:c.1218-9del MANE Select NP_000738.2:n.1218-9del