Canonical Allele Identifier: CA1589086552
Gene: POU4F3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.146339664C= , CM000667.2:g.146339664C= GRCh38
NC_000005.9:g.145719227C= , CM000667.1:g.145719227C= GRCh37
NC_000005.8:g.145699420C= NCBI36
NG_011885.1:g.5641C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000646991.2:c.237C= MANE Select ENSP00000495718.1:p.Thr79=
ENST00000230732.4:c.237C= ENSP00000230732.4:p.Thr79=
NM_002700.2:c.237C= NP_002691.1:p.Thr79=
NM_002700.3:c.237C= MANE Select NP_002691.1:p.Thr79=
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