Canonical Allele Identifier: CA2666629238
Gene: POU1F1 HGNC NCBI

Linked Data

gnomAD v4: 3-87259661-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87259661T>A , CM000665.2:g.87259661T>A GRCh38
NC_000003.11:g.87308811T>A , CM000665.1:g.87308811T>A GRCh37
NC_000003.10:g.87391501T>A NCBI36
NG_008225.2:g.21927A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000344265.8:c.*233A>T ENSP00000342931.3:n.*233A>T
ENST00000350375.7:c.*233A>T MANE Select ENSP00000263781.2:n.*233A>T
ENST00000350375.6:c.*233A>T ENSP00000263781.2:n.*233A>T
NM_000306.3:c.*233A>T NP_000297.1:n.*233A>T
NM_001122757.2:c.*233A>T NP_001116229.1:n.*233A>T
NM_000306.4:c.*233A>T MANE Select NP_000297.1:n.*233A>T
NM_001122757.3:c.*233A>T NP_001116229.1:n.*233A>T