Canonical Allele Identifier: CA2666629351
Gene: POU1F1 HGNC NCBI

Linked Data

gnomAD v4: 3-87259788-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87259788G>T , CM000665.2:g.87259788G>T GRCh38
NC_000003.11:g.87308938G>T , CM000665.1:g.87308938G>T GRCh37
NC_000003.10:g.87391628G>T NCBI36
NG_008225.2:g.21800C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000344265.8:c.*106C>A ENSP00000342931.3:n.*106C>A
ENST00000350375.7:c.*106C>A MANE Select ENSP00000263781.2:n.*106C>A
ENST00000344265.7:c.*106C>A ENSP00000342931.3:n.*106C>A
ENST00000350375.6:c.*106C>A ENSP00000263781.2:n.*106C>A
NM_000306.3:c.*106C>A NP_000297.1:n.*106C>A
NM_001122757.2:c.*106C>A NP_001116229.1:n.*106C>A
NM_000306.4:c.*106C>A MANE Select NP_000297.1:n.*106C>A
NM_001122757.3:c.*106C>A NP_001116229.1:n.*106C>A
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