ClinGen Allele Registry
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Canonical Allele Identifier:
CA13141342
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr10:g.5996890G>C
GRCh37
chr10:g.6038853G>C
Linked Data - Sequence & Population
gnomAD v2:
10:6038853 G / C
gnomAD v3:
10:5996890 G / C
gnomAD v4:
chr10-5996890-G-C
Joint Max Group AF
0.67973849 (EAS)
Genomes Max Group AF
0.67973849 (EAS)
Linked Data - NCBI & NCI
dbSNP:
6602364
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000010.11:g.5996890G>C , CM000672.2:g.5996890G>C
GRCh38
NC_000010.10:g.6038853G>C , CM000672.1:g.6038853G>C
GRCh37
NC_000010.9:g.6078859G>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'