Canonical Allele Identifier: CA2480925321
Gene: CHRNB2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154571668_154571670delinsTCA , CM000663.2:g.154571668_154571670delinsTCA GRCh38
NC_000001.10:g.154544144_154544146delinsTCA , CM000663.1:g.154544144_154544146delinsTCA GRCh37
NC_000001.9:g.152810768_152810770delinsTCA NCBI36
NG_008027.1:g.8888_8890delinsTCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000368476.4:c.845_847delinsTCA MANE Select ENSP00000357461.3:p.Leu282=
ENST00000636034.1:c.845_847delinsTCA ENSP00000489703.1:p.Leu282=
ENST00000637900.1:c.851_853delinsTCA ENSP00000490474.1:p.Leu284=
ENST00000368476.3:c.845_847delinsTCA ENSP00000357461.3:p.Leu282=
NM_000748.2:c.845_847delinsTCA NP_000739.1:p.Leu282=
XM_017000180.2:c.335_337delinsTCA XP_016855669.1:p.Leu112=
XR_001736952.2:n.1097_1099delinsTCA
NM_000748.3:c.845_847delinsTCA MANE Select NP_000739.1:p.Leu282=
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