Canonical Allele Identifier: CA2666629229
Gene: POU1F1 HGNC NCBI

Linked Data

gnomAD v4: 3-87259648-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87259648T>A , CM000665.2:g.87259648T>A GRCh38
NC_000003.11:g.87308798T>A , CM000665.1:g.87308798T>A GRCh37
NC_000003.10:g.87391488T>A NCBI36
NG_008225.2:g.21940A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000344265.8:c.*246A>T ENSP00000342931.3:n.*246A>T
ENST00000350375.7:c.*246A>T MANE Select ENSP00000263781.2:n.*246A>T
ENST00000350375.6:c.*246A>T ENSP00000263781.2:n.*246A>T
NM_000306.3:c.*246A>T NP_000297.1:n.*246A>T
NM_001122757.2:c.*246A>T NP_001116229.1:n.*246A>T
NM_000306.4:c.*246A>T MANE Select NP_000297.1:n.*246A>T
NM_001122757.3:c.*246A>T NP_001116229.1:n.*246A>T