Canonical Allele Identifier: CA434627019
Gene: POU1F1 HGNC NCBI

Linked Data

dbSNP Id: rs1706573773
MyVariant Identifiers: chr3:g.87313478T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87264328T>C , CM000665.2:g.87264328T>C GRCh38
NC_000003.11:g.87313478T>C , CM000665.1:g.87313478T>C GRCh37
NC_000003.10:g.87396168T>C NCBI36
NG_008225.2:g.17260A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000344265.8:c.477A>G ENSP00000342931.3:p.Glu159=
ENST00000350375.7:c.399A>G MANE Select ENSP00000263781.2:p.Glu133=
ENST00000344265.7:c.477A>G ENSP00000342931.3:p.Glu159=
ENST00000350375.6:c.399A>G ENSP00000263781.2:p.Glu133=
ENST00000560656.1:c.399A>G ENSP00000452610.1:p.Glu133=
ENST00000561167.5:c.215-2093A>G ENSP00000454072.1:n.215-2093A>G
NM_000306.3:c.399A>G NP_000297.1:p.Glu133=
NM_001122757.2:c.477A>G NP_001116229.1:p.Glu159=
NM_000306.4:c.399A>G MANE Select NP_000297.1:p.Glu133=
NM_001122757.3:c.477A>G NP_001116229.1:p.Glu159=