Canonical Allele Identifier: CA13272908
Gene: RPS3AP36 HGNC NCBI
COSMIC:
COSN19623051 (not active)
COSN19746909 (not active)
COSN20281673 (not active)
MyVariant.info:
GRCh38 chr10:g.95595157C>T
GRCh37 chr10:g.97354914C>T
gnomAD v2:
10:97354914 C / T
gnomAD v3:
10:95595157 C / T
gnomAD v4:
chr10-95595157-C-T
Joint Max Group AF 0.54849507 (AMR)
Genomes Max Group AF 0.51731127 (NFE)
Exomes Max Group AF 0.56426751 (AMR)
dbSNP:
498055
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.95595157C>T , CM000672.2:g.95595157C>T GRCh38
NC_000010.10:g.97354914C>T , CM000672.1:g.97354914C>T GRCh37
NC_000010.9:g.97344904C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000398190.2:n.560C>T
Search 100 bp 5'
Search 100 bp 3'