Canonical Allele Identifier: CA3491068
Gene: POU4F3 HGNC NCBI

Linked Data

dbSNP Id: rs775448826
ExAC: 5:145719196 G / T
gnomAD v2: 5-145719196-G-T
gnomAD v3: 5-146339633-G-T
gnomAD v4: 5-146339633-G-T
MyVariant Identifiers: chr5:g.145719196G>T (hg19) chr5:g.146339633G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.146339633G>T , CM000667.2:g.146339633G>T GRCh38
NC_000005.9:g.145719196G>T , CM000667.1:g.145719196G>T GRCh37
NC_000005.8:g.145699389G>T NCBI36
NG_011885.1:g.5610G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000646991.2:c.206G>T MANE Select ENSP00000495718.1:p.Gly69Val
ENST00000230732.4:c.206G>T ENSP00000230732.4:p.Gly69Val
NM_002700.2:c.206G>T NP_002691.1:p.Gly69Val
NM_002700.3:c.206G>T MANE Select NP_002691.1:p.Gly69Val
Search 100 bp 5'
Search 100 bp 3'