Canonical Allele Identifier: CA12182104
Gene: PERPP3 HGNC NCBI
MyVariant.info:
GRCh38 chr6:g.16161194A>G
GRCh37 chr6:g.16161425A>G
gnomAD v2:
6:16161425 A / G
gnomAD v3:
6:16161194 A / G
gnomAD v4:
chr6-16161194-A-G
Joint Max Group AF 0.71494646 (EAS)
Genomes Max Group AF 0.70839768 (EAS)
Exomes Max Group AF 0.70985016 (EAS)
dbSNP:
6924995
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.16161194A>G , CM000668.2:g.16161194A>G GRCh38
NC_000006.11:g.16161425A>G , CM000668.1:g.16161425A>G GRCh37
NC_000006.10:g.16269404A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000407522.1:n.269A>G
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