Canonical Allele Identifier: CA2480927352
Gene: CHRNB2 HGNC NCBI

Linked Data

dbSNP Id: rs1696276148

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154576262_154576272del , CM000663.2:g.154576262_154576272del GRCh38
NC_000001.10:g.154548738_154548748del , CM000663.1:g.154548738_154548748del GRCh37
NC_000001.9:g.152815362_152815372del NCBI36
NG_008027.1:g.13482_13492del

Transcript Alleles

HGVS Amino-acid change
ENST00000368476.4:c.*330_*340del MANE Select ENSP00000357461.3:n.*330_*340del
ENST00000636034.1:c.1505+334_1505+344del ENSP00000489703.1:n.1505+334_1505+344del
ENST00000637900.1:c.*330_*340del ENSP00000490474.1:n.*330_*340del
ENST00000368476.3:c.*330_*340del ENSP00000357461.3:n.*330_*340del
NM_000748.2:c.*330_*340del NP_000739.1:n.*330_*340del
XM_017000180.2:c.*330_*340del XP_016855669.1:n.*330_*340del
XR_001736952.2:n.2091_2101del
NM_000748.3:c.*330_*340del MANE Select NP_000739.1:n.*330_*340del