Canonical Allele Identifier: CA2000234314
Gene: POU2AF1 HGNC NCBI

Linked Data

dbSNP Id: rs1591185402

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.111352410T>G , CM000673.2:g.111352410T>G GRCh38
NC_000011.9:g.111223135T>G , CM000673.1:g.111223135T>G GRCh37
NC_000011.8:g.110728345T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000393067.8:c.*1851A>C MANE Select ENSP00000376786.3:n.*1851A>C
ENST00000393067.7:c.*1851A>C ENSP00000376786.3:n.*1851A>C
NM_006235.2:c.*1851A>C NP_006226.2:n.*1851A>C
XM_005271593.1:c.*1851A>C XP_005271650.1:n.*1851A>C
XM_005271594.3:c.*1851A>C XP_005271651.1:n.*1851A>C
XM_006718859.1:c.*1851A>C XP_006718922.1:n.*1851A>C
XM_005271593.2:c.*1851A>C XP_005271650.1:n.*1851A>C
XM_006718860.4:c.*4006A>C XP_006718923.1:n.*4006A>C
XM_017017932.1:c.*4006A>C XP_016873421.1:n.*4006A>C
NM_006235.3:c.*1851A>C MANE Select NP_006226.2:n.*1851A>C