Canonical Allele Identifier: CA79036421
Gene: POU1F1 HGNC NCBI

Linked Data

dbSNP Id: rs6792500
MyVariant Identifiers: chr3:g.87259681T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87259681T>C , CM000665.2:g.87259681T>C GRCh38
NG_008225.2:g.21907A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000344265.8:c.*213A>G ENSP00000342931.3:n.*213A>G
ENST00000350375.7:c.*213A>G MANE Select ENSP00000263781.2:n.*213A>G
ENST00000350375.6:c.*213A>G ENSP00000263781.2:n.*213A>G
NM_000306.3:c.*213A>G NP_000297.1:n.*213A>G
NM_001122757.2:c.*213A>G NP_001116229.1:n.*213A>G
NM_000306.4:c.*213A>G MANE Select NP_000297.1:n.*213A>G
NM_001122757.3:c.*213A>G NP_001116229.1:n.*213A>G
Search 100 bp 5'
Search 100 bp 3'