Canonical Allele Identifier: CA2666629699
Gene: POU1F1 HGNC NCBI

Linked Data

gnomAD v4: 3-87261977-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87261977C>T , CM000665.2:g.87261977C>T GRCh38
NC_000003.11:g.87311127C>T , CM000665.1:g.87311127C>T GRCh37
NC_000003.10:g.87393817C>T NCBI36
NG_008225.2:g.19611G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000344265.8:c.682+94G>A ENSP00000342931.3:n.682+94G>A
ENST00000350375.7:c.604+94G>A MANE Select ENSP00000263781.2:n.604+94G>A
ENST00000344265.7:c.682+94G>A ENSP00000342931.3:n.682+94G>A
ENST00000350375.6:c.604+94G>A ENSP00000263781.2:n.604+94G>A
ENST00000560656.1:c.440-1873G>A ENSP00000452610.1:n.440-1873G>A
ENST00000561167.5:c.379+94G>A ENSP00000454072.1:n.379+94G>A
NM_000306.3:c.604+94G>A NP_000297.1:n.604+94G>A
NM_001122757.2:c.682+94G>A NP_001116229.1:n.682+94G>A
NM_000306.4:c.604+94G>A MANE Select NP_000297.1:n.604+94G>A
NM_001122757.3:c.682+94G>A NP_001116229.1:n.682+94G>A