Canonical Allele Identifier: CA79036438
Gene: POU1F1 HGNC NCBI

Linked Data

dbSNP Id: rs768535274
MyVariant Identifiers: chr3:g.87308947A>G (hg19) chr3:g.87259797A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87259797A>G , CM000665.2:g.87259797A>G GRCh38
NC_000003.11:g.87308947A>G , CM000665.1:g.87308947A>G GRCh37
NC_000003.10:g.87391637A>G NCBI36
NG_008225.2:g.21791T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000344265.8:c.*97T>C ENSP00000342931.3:n.*97T>C
ENST00000350375.7:c.*97T>C MANE Select ENSP00000263781.2:n.*97T>C
ENST00000344265.7:c.*97T>C ENSP00000342931.3:n.*97T>C
ENST00000350375.6:c.*97T>C ENSP00000263781.2:n.*97T>C
NM_000306.3:c.*97T>C NP_000297.1:n.*97T>C
NM_001122757.2:c.*97T>C NP_001116229.1:n.*97T>C
NM_000306.4:c.*97T>C MANE Select NP_000297.1:n.*97T>C
NM_001122757.3:c.*97T>C NP_001116229.1:n.*97T>C
Search 100 bp 5'
Search 100 bp 3'