Canonical Allele Identifier: CA911575195
Gene: POU1F1 HGNC NCBI

Linked Data

dbSNP Id: rs1369180879
gnomAD v4: 3-87259831-T-G
MyVariant Identifiers: chr3:g.87308981T>G (hg19) chr3:g.87259831T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87259831T>G , CM000665.2:g.87259831T>G GRCh38
NC_000003.11:g.87308981T>G , CM000665.1:g.87308981T>G GRCh37
NC_000003.10:g.87391671T>G NCBI36
NG_008225.2:g.21757A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000344265.8:c.*63A>C ENSP00000342931.3:n.*63A>C
ENST00000350375.7:c.*63A>C MANE Select ENSP00000263781.2:n.*63A>C
ENST00000344265.7:c.*63A>C ENSP00000342931.3:n.*63A>C
ENST00000350375.6:c.*63A>C ENSP00000263781.2:n.*63A>C
NM_000306.3:c.*63A>C NP_000297.1:n.*63A>C
NM_001122757.2:c.*63A>C NP_001116229.1:n.*63A>C
NM_000306.4:c.*63A>C MANE Select NP_000297.1:n.*63A>C
NM_001122757.3:c.*63A>C NP_001116229.1:n.*63A>C
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