Canonical Allele Identifier: CA353693816
Gene: POU1F1 HGNC NCBI

Linked Data

dbSNP Id: rs1706575495
gnomAD v4: 3-87264363-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87264363T>C , CM000665.2:g.87264363T>C GRCh38
NC_000003.11:g.87313513T>C , CM000665.1:g.87313513T>C GRCh37
NC_000003.10:g.87396203T>C NCBI36
NG_008225.2:g.17225A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000344265.8:c.442A>G ENSP00000342931.3:p.Ile148Val
ENST00000350375.7:c.364A>G MANE Select ENSP00000263781.2:p.Ile122Val
ENST00000344265.7:c.442A>G ENSP00000342931.3:p.Ile148Val
ENST00000350375.6:c.364A>G ENSP00000263781.2:p.Ile122Val
ENST00000560656.1:c.364A>G ENSP00000452610.1:p.Ile122Val
ENST00000561167.5:c.215-2128A>G ENSP00000454072.1:n.215-2128A>G
NM_000306.3:c.364A>G NP_000297.1:p.Ile122Val
NM_001122757.2:c.442A>G NP_001116229.1:p.Ile148Val
NM_000306.4:c.364A>G MANE Select NP_000297.1:p.Ile122Val
NM_001122757.3:c.442A>G NP_001116229.1:p.Ile148Val