Canonical Allele Identifier: CA1381566333
Gene: POU1F1 HGNC NCBI

Linked Data

dbSNP Id: rs1017321733

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87261904T>C , CM000665.2:g.87261904T>C GRCh38
NC_000003.11:g.87311054T>C , CM000665.1:g.87311054T>C GRCh37
NC_000003.10:g.87393744T>C NCBI36
NG_008225.2:g.19684A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000344265.8:c.682+167A>G ENSP00000342931.3:n.682+167A>G
ENST00000350375.7:c.604+167A>G MANE Select ENSP00000263781.2:n.604+167A>G
ENST00000344265.7:c.682+167A>G ENSP00000342931.3:n.682+167A>G
ENST00000350375.6:c.604+167A>G ENSP00000263781.2:n.604+167A>G
ENST00000560656.1:c.440-1800A>G ENSP00000452610.1:n.440-1800A>G
ENST00000561167.5:c.379+167A>G ENSP00000454072.1:n.379+167A>G
NM_000306.3:c.604+167A>G NP_000297.1:n.604+167A>G
NM_001122757.2:c.682+167A>G NP_001116229.1:n.682+167A>G
NM_000306.4:c.604+167A>G MANE Select NP_000297.1:n.604+167A>G
NM_001122757.3:c.682+167A>G NP_001116229.1:n.682+167A>G