Canonical Allele Identifier: CA2675813810
Gene: POU4F3 HGNC NCBI

Linked Data

gnomAD v4: 5-146339462-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.146339462A>C , CM000667.2:g.146339462A>C GRCh38
NC_000005.9:g.145719025A>C , CM000667.1:g.145719025A>C GRCh37
NC_000005.8:g.145699218A>C NCBI36
NG_011885.1:g.5439A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000646991.2:c.121-86A>C MANE Select ENSP00000495718.1:n.121-86A>C
ENST00000230732.4:c.121-86A>C ENSP00000230732.4:n.121-86A>C
NM_002700.2:c.121-86A>C NP_002691.1:n.121-86A>C
NM_002700.3:c.121-86A>C MANE Select NP_002691.1:n.121-86A>C
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