Canonical Allele Identifier: CA447098104
Gene: POU4F3 HGNC NCBI

Linked Data

dbSNP Id: rs1760434198
MyVariant Identifiers: chr5:g.145719797C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.146340234C>T , CM000667.2:g.146340234C>T GRCh38
NC_000005.9:g.145719797C>T , CM000667.1:g.145719797C>T GRCh37
NC_000005.8:g.145699990C>T NCBI36
NG_011885.1:g.6211C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000646991.2:c.807C>T MANE Select ENSP00000495718.1:p.Phe269=
ENST00000230732.4:c.807C>T ENSP00000230732.4:p.Phe269=
NM_002700.2:c.807C>T NP_002691.1:p.Phe269=
NM_002700.3:c.807C>T MANE Select NP_002691.1:p.Phe269=
Search 100 bp 5'
Search 100 bp 3'