Canonical Allele Identifier: CA1381563654
Gene: POU1F1 HGNC NCBI

Linked Data

dbSNP Id: rs1706467371
gnomAD v4: 3-87259662-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87259662A>G , CM000665.2:g.87259662A>G GRCh38
NC_000003.11:g.87308812A>G , CM000665.1:g.87308812A>G GRCh37
NC_000003.10:g.87391502A>G NCBI36
NG_008225.2:g.21926T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000344265.8:c.*232T>C ENSP00000342931.3:n.*232T>C
ENST00000350375.7:c.*232T>C MANE Select ENSP00000263781.2:n.*232T>C
ENST00000350375.6:c.*232T>C ENSP00000263781.2:n.*232T>C
NM_000306.3:c.*232T>C NP_000297.1:n.*232T>C
NM_001122757.2:c.*232T>C NP_001116229.1:n.*232T>C
NM_000306.4:c.*232T>C MANE Select NP_000297.1:n.*232T>C
NM_001122757.3:c.*232T>C NP_001116229.1:n.*232T>C