Canonical Allele Identifier: CA15597864
Gene: PUM3 HGNC NCBI
COSMIC:
COSN14917634 (not active)
MyVariant.info:
GRCh38 chr9:g.2742771T>C
GRCh37 chr9:g.2742771T>C
gnomAD v2:
9:2742771 T / C
gnomAD v3:
9:2742771 T / C
gnomAD v4:
chr9-2742771-T-C
Joint Max Group AF 0.70413422 (AFR)
Genomes Max Group AF 0.70413422 (AFR)
dbSNP:
2034764
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.2742771T>C , CM000671.2:g.2742771T>C GRCh38
NC_000009.11:g.2742771T>C , CM000671.1:g.2742771T>C GRCh37
NC_000009.10:g.2732771T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000490444.2:c.277-22239A>G ENSP00000474467.1:n.277-22239A>G
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