Canonical Allele Identifier: CA15595079
Gene: PBX3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.125766699T>A , CM000671.2:g.125766699T>A GRCh38
NC_000009.11:g.128528978T>A , CM000671.1:g.128528978T>A GRCh37
NC_000009.10:g.127568799T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000373489.10:c.274+18076T>A MANE Select ENSP00000362588.5:n.274+18076T>A
ENST00000672674.1:n.339-11283T>A
ENST00000673571.1:n.37+16189T>A
ENST00000342287.9:c.274+18076T>A ENSP00000341990.5:n.274+18076T>A
ENST00000373482.6:c.274+18076T>A ENSP00000362581.2:n.274+18076T>A
ENST00000373487.8:c.274+18076T>A ENSP00000362586.4:n.274+18076T>A
ENST00000373489.9:c.274+18076T>A ENSP00000362588.5:n.274+18076T>A
ENST00000373492.6:c.274+18076T>A ENSP00000362591.2:n.274+18076T>A
ENST00000447726.6:c.49+18076T>A ENSP00000387456.2:n.49+18076T>A
ENST00000491787.7:c.49+18076T>A ENSP00000475679.1:n.49+18076T>A
ENST00000497091.1:n.354+18076T>A
NM_001134778.1:c.49+18076T>A NP_001128250.1:n.49+18076T>A
NM_006195.5:c.274+18076T>A NP_006186.1:n.274+18076T>A
NR_024122.1:n.390+18076T>A
NR_024123.1:n.390+18076T>A
XM_006717130.1:c.274+18076T>A XP_006717193.1:n.274+18076T>A
XM_006717131.1:c.274+18076T>A XP_006717194.1:n.274+18076T>A
XM_006717132.1:c.274+18076T>A XP_006717195.1:n.274+18076T>A
XM_006717133.1:c.-28+18076T>A XP_006717196.1:n.-28+18076T>A
XM_011518755.1:c.49+18076T>A XP_011517057.1:n.49+18076T>A
NM_001330782.1:c.274+18076T>A NP_001317711.1:n.274+18076T>A
XM_006717133.2:c.-28+18076T>A XP_006717196.1:n.-28+18076T>A
XM_011518755.2:c.49+18076T>A XP_011517057.1:n.49+18076T>A
XM_017014786.1:c.49+18076T>A XP_016870275.1:n.49+18076T>A
NM_006195.6:c.274+18076T>A MANE Select NP_006186.1:n.274+18076T>A
NM_001134778.2:c.49+18076T>A NP_001128250.1:n.49+18076T>A
NM_001330782.2:c.274+18076T>A NP_001317711.1:n.274+18076T>A
NR_024122.2:n.355+18076T>A
NR_024123.2:n.355+18076T>A
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