Canonical Allele Identifier: CA361620489
Gene: POU4F3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.145719322T>C (hg19) chr5:g.146339759T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.146339759T>C , CM000667.2:g.146339759T>C GRCh38
NC_000005.9:g.145719322T>C , CM000667.1:g.145719322T>C GRCh37
NC_000005.8:g.145699515T>C NCBI36
NG_011885.1:g.5736T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000646991.2:c.332T>C MANE Select ENSP00000495718.1:p.Val111Ala
ENST00000230732.4:c.332T>C ENSP00000230732.4:p.Val111Ala
NM_002700.2:c.332T>C NP_002691.1:p.Val111Ala
NM_002700.3:c.332T>C MANE Select NP_002691.1:p.Val111Ala
Search 100 bp 5'
Search 100 bp 3'