Canonical Allele Identifier: CA353692753
Gene: POU1F1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.87311248A>T (hg19) chr3:g.87262098A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87262098A>T , CM000665.2:g.87262098A>T GRCh38
NC_000003.11:g.87311248A>T , CM000665.1:g.87311248A>T GRCh37
NC_000003.10:g.87393938A>T NCBI36
NG_008225.2:g.19490T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000344265.8:c.655T>A ENSP00000342931.3:p.Trp219Arg
ENST00000350375.7:c.577T>A MANE Select ENSP00000263781.2:p.Trp193Arg
ENST00000344265.7:c.655T>A ENSP00000342931.3:p.Trp219Arg
ENST00000350375.6:c.577T>A ENSP00000263781.2:p.Trp193Arg
ENST00000560656.1:c.440-1994T>A ENSP00000452610.1:n.440-1994T>A
ENST00000561167.5:c.352T>A ENSP00000454072.1:p.Trp118Arg
NM_000306.3:c.577T>A NP_000297.1:p.Trp193Arg
NM_001122757.2:c.655T>A NP_001116229.1:p.Trp219Arg
NM_000306.4:c.577T>A MANE Select NP_000297.1:p.Trp193Arg
NM_001122757.3:c.655T>A NP_001116229.1:p.Trp219Arg
Search 100 bp 5'
Search 100 bp 3'