Canonical Allele Identifier: CA2000234302
Gene: POU2AF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.111352393A= , CM000673.2:g.111352393A= GRCh38
NC_000011.9:g.111223118A= , CM000673.1:g.111223118A= GRCh37
NC_000011.8:g.110728328A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000393067.8:c.*1868T= MANE Select ENSP00000376786.3:n.*1868T=
ENST00000393067.7:c.*1868T= ENSP00000376786.3:n.*1868T=
NM_006235.2:c.*1868T= NP_006226.2:n.*1868T=
XM_005271593.1:c.*1868T= XP_005271650.1:n.*1868T=
XM_005271594.3:c.*1868T= XP_005271651.1:n.*1868T=
XM_006718859.1:c.*1868T= XP_006718922.1:n.*1868T=
XM_005271593.2:c.*1868T= XP_005271650.1:n.*1868T=
XM_006718860.4:c.*4023T= XP_006718923.1:n.*4023T=
XM_017017932.1:c.*4023T= XP_016873421.1:n.*4023T=
NM_006235.3:c.*1868T= MANE Select NP_006226.2:n.*1868T=