Canonical Allele Identifier: CA434579393
Gene: POU1F1 HGNC NCBI

Linked Data

gnomAD v4: 3-87259966-T-C
MyVariant Identifiers: chr3:g.87309116T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87259966T>C , CM000665.2:g.87259966T>C GRCh38
NC_000003.11:g.87309116T>C , CM000665.1:g.87309116T>C GRCh37
NC_000003.10:g.87391806T>C NCBI36
NG_008225.2:g.21622A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000344265.8:c.882A>G ENSP00000342931.3:p.Arg294=
ENST00000350375.7:c.804A>G MANE Select ENSP00000263781.2:p.Arg268=
ENST00000344265.7:c.882A>G ENSP00000342931.3:p.Arg294=
ENST00000350375.6:c.804A>G ENSP00000263781.2:p.Arg268=
ENST00000560656.1:c.578A>G ENSP00000452610.1:n.578A>G
ENST00000561167.5:c.579A>G ENSP00000454072.1:p.Arg193=
NM_000306.3:c.804A>G NP_000297.1:p.Arg268=
NM_001122757.2:c.882A>G NP_001116229.1:p.Arg294=
NM_000306.4:c.804A>G MANE Select NP_000297.1:p.Arg268=
NM_001122757.3:c.882A>G NP_001116229.1:p.Arg294=