Canonical Allele Identifier: CA2615915598
Gene: POU2AF1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.111352392G>C , CM000673.2:g.111352392G>C GRCh38
NC_000011.9:g.111223117G>C , CM000673.1:g.111223117G>C GRCh37
NC_000011.8:g.110728327G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000393067.8:c.*1869C>G MANE Select ENSP00000376786.3:n.*1869C>G
ENST00000393067.7:c.*1869C>G ENSP00000376786.3:n.*1869C>G
NM_006235.2:c.*1869C>G NP_006226.2:n.*1869C>G
XM_005271593.1:c.*1869C>G XP_005271650.1:n.*1869C>G
XM_005271594.3:c.*1869C>G XP_005271651.1:n.*1869C>G
XM_006718859.1:c.*1869C>G XP_006718922.1:n.*1869C>G
XM_005271593.2:c.*1869C>G XP_005271650.1:n.*1869C>G
XM_006718860.4:c.*4024C>G XP_006718923.1:n.*4024C>G
XM_017017932.1:c.*4024C>G XP_016873421.1:n.*4024C>G
NM_006235.3:c.*1869C>G MANE Select NP_006226.2:n.*1869C>G