Canonical Allele Identifier: CA2480925174
Gene: CHRNB2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154571172_154571173delinsTG , CM000663.2:g.154571172_154571173delinsTG GRCh38
NC_000001.10:g.154543648_154543649delinsTG , CM000663.1:g.154543648_154543649delinsTG GRCh37
NC_000001.9:g.152810272_152810273delinsTG NCBI36
NG_008027.1:g.8392_8393delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000368476.4:c.366-17_366-16delinsTG MANE Select ENSP00000357461.3:n.366-17_366-16delinsTG
ENST00000636034.1:c.366-17_366-16delinsTG ENSP00000489703.1:n.366-17_366-16delinsTG
ENST00000637900.1:c.372-17_372-16delinsTG ENSP00000490474.1:n.372-17_372-16delinsTG
ENST00000368476.3:c.366-17_366-16delinsTG ENSP00000357461.3:n.366-17_366-16delinsTG
NM_000748.2:c.366-17_366-16delinsTG NP_000739.1:n.366-17_366-16delinsTG
XM_017000180.2:c.-9-153_-9-152delinsTG XP_016855669.1:n.-9-153_-9-152delinsTG
XR_001736952.2:n.618-17_618-16delinsTG
NM_000748.3:c.366-17_366-16delinsTG MANE Select NP_000739.1:n.366-17_366-16delinsTG
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