Canonical Allele Identifier: CA889604097
Gene: CHRNB2 HGNC NCBI

Linked Data

dbSNP Id: rs1398892264

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154576257_154576268del , CM000663.2:g.154576257_154576268del GRCh38
NC_000001.10:g.154548733_154548744del , CM000663.1:g.154548733_154548744del GRCh37
NC_000001.9:g.152815357_152815368del NCBI36
NG_008027.1:g.13477_13488del

Transcript Alleles

HGVS Amino-acid change
ENST00000368476.4:c.*325_*336del MANE Select ENSP00000357461.3:n.*325_*336del
ENST00000636034.1:c.1505+329_1505+340del ENSP00000489703.1:n.1505+329_1505+340del
ENST00000637900.1:c.*325_*336del ENSP00000490474.1:n.*325_*336del
ENST00000368476.3:c.*325_*336del ENSP00000357461.3:n.*325_*336del
NM_000748.2:c.*325_*336del NP_000739.1:n.*325_*336del
XM_017000180.2:c.*325_*336del XP_016855669.1:n.*325_*336del
XR_001736952.2:n.2086_2097del
NM_000748.3:c.*325_*336del MANE Select NP_000739.1:n.*325_*336del