Canonical Allele Identifier: CA2648173043
Gene: CHRNB2 HGNC NCBI

Linked Data

gnomAD v4: 1-154576078-CCCA-C
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154576080_154576082del , CM000663.2:g.154576080_154576082del GRCh38
NC_000001.10:g.154548556_154548558del , CM000663.1:g.154548556_154548558del GRCh37
NC_000001.9:g.152815180_152815182del NCBI36
NG_008027.1:g.13300_13302del

Transcript Alleles

HGVS Amino-acid Change
ENST00000368476.4:c.*148_*150del MANE Select ENSP00000357461.3:n.*148_*150del
ENST00000636034.1:c.1505+152_1505+154del ENSP00000489703.1:n.1505+152_1505+154del
ENST00000637900.1:c.*148_*150del ENSP00000490474.1:n.*148_*150del
ENST00000368476.3:c.*148_*150del ENSP00000357461.3:n.*148_*150del
NM_000748.2:c.*148_*150del NP_000739.1:n.*148_*150del
XM_017000180.2:c.*148_*150del XP_016855669.1:n.*148_*150del
XR_001736952.2:n.1909_1911del
NM_000748.3:c.*148_*150del MANE Select NP_000739.1:n.*148_*150del
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