Canonical Allele Identifier: CA3491160
Gene: POU4F3 HGNC NCBI

Linked Data

dbSNP Id: rs778970237
ExAC: 5:145719523 G / C
gnomAD v2: 5-145719523-G-C
gnomAD v4: 5-146339960-G-C
MyVariant Identifiers: chr5:g.145719523G>C (hg19) chr5:g.146339960G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.146339960G>C , CM000667.2:g.146339960G>C GRCh38
NC_000005.9:g.145719523G>C , CM000667.1:g.145719523G>C GRCh37
NC_000005.8:g.145699716G>C NCBI36
NG_011885.1:g.5937G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000646991.2:c.533G>C MANE Select ENSP00000495718.1:p.Ser178Thr
ENST00000230732.4:c.533G>C ENSP00000230732.4:p.Ser178Thr
NM_002700.2:c.533G>C NP_002691.1:p.Ser178Thr
NM_002700.3:c.533G>C MANE Select NP_002691.1:p.Ser178Thr
Search 100 bp 5'
Search 100 bp 3'