Canonical Allele Identifier: CA128860330
Gene: POU4F3 HGNC NCBI

Linked Data

dbSNP Id: rs1001975970
gnomAD v4: 5-146339400-C-T
MyVariant Identifiers: chr5:g.145718963C>T (hg19) chr5:g.146339400C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.146339400C>T , CM000667.2:g.146339400C>T GRCh38
NC_000005.9:g.145718963C>T , CM000667.1:g.145718963C>T GRCh37
NC_000005.8:g.145699156C>T NCBI36
NG_011885.1:g.5377C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000646991.2:c.121-148C>T MANE Select ENSP00000495718.1:n.121-148C>T
ENST00000230732.4:c.121-148C>T ENSP00000230732.4:n.121-148C>T
NM_002700.2:c.121-148C>T NP_002691.1:n.121-148C>T
NM_002700.3:c.121-148C>T MANE Select NP_002691.1:n.121-148C>T
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