Canonical Allele Identifier: CA361622643
Gene: POU4F3 HGNC NCBI

Linked Data

dbSNP Id: rs2126961905
MyVariant Identifiers: chr5:g.145719822C>A (hg19) chr5:g.146340259C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.146340259C>A , CM000667.2:g.146340259C>A GRCh38
NC_000005.9:g.145719822C>A , CM000667.1:g.145719822C>A GRCh37
NC_000005.8:g.145700015C>A NCBI36
NG_011885.1:g.6236C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000646991.2:c.832C>A MANE Select ENSP00000495718.1:p.Arg278Ser
ENST00000230732.4:c.832C>A ENSP00000230732.4:p.Arg278Ser
NM_002700.2:c.832C>A NP_002691.1:p.Arg278Ser
NM_002700.3:c.832C>A MANE Select NP_002691.1:p.Arg278Ser
Search 100 bp 5'
Search 100 bp 3'