Canonical Allele Identifier: CA916315127
Gene: CHRNB2 HGNC NCBI

Linked Data

dbSNP Id: rs1557851805
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154571714_154571728del , CM000663.2:g.154571714_154571728del GRCh38
NC_000001.10:g.154544190_154544204del , CM000663.1:g.154544190_154544204del GRCh37
NC_000001.9:g.152810814_152810828del NCBI36
NG_008027.1:g.8934_8948del

Transcript Alleles

HGVS Amino-acid Change
ENST00000368476.4:c.891_905del MANE Select ENSP00000357461.3:p.Gly298_Met302del
ENST00000636034.1:c.891_905del ENSP00000489703.1:p.Gly298_Met302del
ENST00000637900.1:c.897_911del ENSP00000490474.1:p.Gly300_Met304del
ENST00000368476.3:c.891_905del ENSP00000357461.3:p.Gly298_Met302del
NM_000748.2:c.891_905del NP_000739.1:p.Gly298_Met302del
XM_017000180.2:c.381_395del XP_016855669.1:p.Gly128_Met132del
XR_001736952.2:n.1143_1157del
NM_000748.3:c.891_905del MANE Select NP_000739.1:p.Gly298_Met302del
Search 100 bp 5'
Search 100 bp 3'