ClinGen Allele Registry
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Canonical Allele Identifier:
CA13179372
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr10:g.4108929T>G
GRCh37
chr10:g.4151121T>G
Linked Data - Sequence & Population
gnomAD v2:
10:4151121 T / G
gnomAD v3:
10:4108929 T / G
gnomAD v4:
chr10-4108929-T-G
Joint Max Group AF
0.34584307 (AFR)
Genomes Max Group AF
0.34584307 (AFR)
Linked Data - NCBI & NCI
dbSNP:
10795130
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000010.11:g.4108929T>G , CM000672.2:g.4108929T>G
GRCh38
NC_000010.10:g.4151121T>G , CM000672.1:g.4151121T>G
GRCh37
NC_000010.9:g.4141121T>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'