Canonical Allele Identifier: CA361622698
Gene: POU4F3 HGNC NCBI

Linked Data

dbSNP Id: rs1449371669
COSMIC: COSM736505
MyVariant Identifiers: chr5:g.145719834G>A (hg19) chr5:g.146340271G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.146340271G>A , CM000667.2:g.146340271G>A GRCh38
NC_000005.9:g.145719834G>A , CM000667.1:g.145719834G>A GRCh37
NC_000005.8:g.145700027G>A NCBI36
NG_011885.1:g.6248G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000646991.2:c.844G>A MANE Select ENSP00000495718.1:p.Ala282Thr
ENST00000230732.4:c.844G>A ENSP00000230732.4:p.Ala282Thr
NM_002700.2:c.844G>A NP_002691.1:p.Ala282Thr
NM_002700.3:c.844G>A MANE Select NP_002691.1:p.Ala282Thr
Search 100 bp 5'
Search 100 bp 3'