Canonical Allele Identifier: CA2666629376
Gene: POU1F1 HGNC NCBI

Linked Data

gnomAD v4: 3-87259855-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87259855T>G , CM000665.2:g.87259855T>G GRCh38
NC_000003.11:g.87309005T>G , CM000665.1:g.87309005T>G GRCh37
NC_000003.10:g.87391695T>G NCBI36
NG_008225.2:g.21733A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000344265.8:c.*39A>C ENSP00000342931.3:n.*39A>C
ENST00000350375.7:c.*39A>C MANE Select ENSP00000263781.2:n.*39A>C
ENST00000344265.7:c.*39A>C ENSP00000342931.3:n.*39A>C
ENST00000350375.6:c.*39A>C ENSP00000263781.2:n.*39A>C
NM_000306.3:c.*39A>C NP_000297.1:n.*39A>C
NM_001122757.2:c.*39A>C NP_001116229.1:n.*39A>C
NM_000306.4:c.*39A>C MANE Select NP_000297.1:n.*39A>C
NM_001122757.3:c.*39A>C NP_001116229.1:n.*39A>C
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