Canonical Allele Identifier: CA2000234277
Gene: POU2AF1 HGNC NCBI

Linked Data

dbSNP Id: rs1860740080
gnomAD v4: 11-111352330-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.111352330C>T , CM000673.2:g.111352330C>T GRCh38
NC_000011.9:g.111223055C>T , CM000673.1:g.111223055C>T GRCh37
NC_000011.8:g.110728265C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000393067.8:c.*1931G>A MANE Select ENSP00000376786.3:n.*1931G>A
ENST00000393067.7:c.*1931G>A ENSP00000376786.3:n.*1931G>A
NM_006235.2:c.*1931G>A NP_006226.2:n.*1931G>A
XM_005271593.1:c.*1931G>A XP_005271650.1:n.*1931G>A
XM_005271594.3:c.*1931G>A XP_005271651.1:n.*1931G>A
XM_006718859.1:c.*1931G>A XP_006718922.1:n.*1931G>A
XM_005271593.2:c.*1931G>A XP_005271650.1:n.*1931G>A
XM_006718860.4:c.*4086G>A XP_006718923.1:n.*4086G>A
XM_017017932.1:c.*4086G>A XP_016873421.1:n.*4086G>A
NM_006235.3:c.*1931G>A MANE Select NP_006226.2:n.*1931G>A
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