Canonical Allele Identifier: CA2000234256
Gene: POU2AF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.111352278G= , CM000673.2:g.111352278G= GRCh38
NC_000011.9:g.111223003G= , CM000673.1:g.111223003G= GRCh37
NC_000011.8:g.110728213G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000393067.8:c.*1983C= MANE Select ENSP00000376786.3:n.*1983C=
ENST00000393067.7:c.*1983C= ENSP00000376786.3:n.*1983C=
NM_006235.2:c.*1983C= NP_006226.2:n.*1983C=
XM_005271593.1:c.*1983C= XP_005271650.1:n.*1983C=
XM_005271594.3:c.*1983C= XP_005271651.1:n.*1983C=
XM_006718859.1:c.*1983C= XP_006718922.1:n.*1983C=
XM_005271593.2:c.*1983C= XP_005271650.1:n.*1983C=
XM_006718860.4:c.*4138C= XP_006718923.1:n.*4138C=
XM_017017932.1:c.*4138C= XP_016873421.1:n.*4138C=
NM_006235.3:c.*1983C= MANE Select NP_006226.2:n.*1983C=