Canonical Allele Identifier: CA434627034
Gene: POU1F1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.87313489T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87264339T>G , CM000665.2:g.87264339T>G GRCh38
NC_000003.11:g.87313489T>G , CM000665.1:g.87313489T>G GRCh37
NC_000003.10:g.87396179T>G NCBI36
NG_008225.2:g.17249A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000344265.8:c.466A>C ENSP00000342931.3:p.Arg156=
ENST00000350375.7:c.388A>C MANE Select ENSP00000263781.2:p.Arg130=
ENST00000344265.7:c.466A>C ENSP00000342931.3:p.Arg156=
ENST00000350375.6:c.388A>C ENSP00000263781.2:p.Arg130=
ENST00000560656.1:c.388A>C ENSP00000452610.1:p.Arg130=
ENST00000561167.5:c.215-2104A>C ENSP00000454072.1:n.215-2104A>C
NM_000306.3:c.388A>C NP_000297.1:p.Arg130=
NM_001122757.2:c.466A>C NP_001116229.1:p.Arg156=
NM_000306.4:c.388A>C MANE Select NP_000297.1:p.Arg130=
NM_001122757.3:c.466A>C NP_001116229.1:p.Arg156=