Canonical Allele Identifier: CA2480925344
Gene: CHRNB2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154571698_154571701delinsTCGA , CM000663.2:g.154571698_154571701delinsTCGA GRCh38
NC_000001.10:g.154544174_154544177delinsTCGA , CM000663.1:g.154544174_154544177delinsTCGA GRCh37
NC_000001.9:g.152810798_152810801delinsTCGA NCBI36
NG_008027.1:g.8918_8921delinsTCGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000368476.4:c.875_878delinsTCGA MANE Select ENSP00000357461.3:p.Leu292=
ENST00000636034.1:c.875_878delinsTCGA ENSP00000489703.1:p.Leu292=
ENST00000637900.1:c.881_884delinsTCGA ENSP00000490474.1:p.Leu294=
ENST00000368476.3:c.875_878delinsTCGA ENSP00000357461.3:p.Leu292=
NM_000748.2:c.875_878delinsTCGA NP_000739.1:p.Leu292=
XM_017000180.2:c.365_368delinsTCGA XP_016855669.1:p.Leu122=
XR_001736952.2:n.1127_1130delinsTCGA
NM_000748.3:c.875_878delinsTCGA MANE Select NP_000739.1:p.Leu292=
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