Canonical Allele Identifier: CA671710399

Gene: POU2AF1

Linked Data

• dbSNP Id: rs1405253542
• MyVariant Identifiers: chr11:g.111223146G>C (hg19) ; chr11:g.111352421G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.111352421G>C , CM000673.2:g.111352421G>C	GRCh38
NC_000011.9:g.111223146G>C , CM000673.1:g.111223146G>C	GRCh37
NC_000011.8:g.110728356G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393067.8:c.*1840C>G MANE Select	ENSP00000376786.3:n.*1840C>G
ENST00000393067.7:c.*1840C>G	ENSP00000376786.3:n.*1840C>G
NM_006235.2:c.*1840C>G	NP_006226.2:n.*1840C>G
XM_005271593.1:c.*1840C>G	XP_005271650.1:n.*1840C>G
XM_005271594.3:c.*1840C>G	XP_005271651.1:n.*1840C>G
XM_006718859.1:c.*1840C>G	XP_006718922.1:n.*1840C>G
XM_005271593.2:c.*1840C>G	XP_005271650.1:n.*1840C>G
XM_006718860.4:c.*3995C>G	XP_006718923.1:n.*3995C>G
XM_017017932.1:c.*3995C>G	XP_016873421.1:n.*3995C>G
NM_006235.3:c.*1840C>G MANE Select	NP_006226.2:n.*1840C>G