Canonical Allele Identifier: CA361620646
Gene: POU4F3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.145719402T>A (hg19) chr5:g.146339839T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.146339839T>A , CM000667.2:g.146339839T>A GRCh38
NC_000005.9:g.145719402T>A , CM000667.1:g.145719402T>A GRCh37
NC_000005.8:g.145699595T>A NCBI36
NG_011885.1:g.5816T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000646991.2:c.412T>A MANE Select ENSP00000495718.1:p.Ser138Thr
ENST00000230732.4:c.412T>A ENSP00000230732.4:p.Ser138Thr
NM_002700.2:c.412T>A NP_002691.1:p.Ser138Thr
NM_002700.3:c.412T>A MANE Select NP_002691.1:p.Ser138Thr
Search 100 bp 5'
Search 100 bp 3'