ClinGen Allele Registry
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Canonical Allele Identifier:
CA13352938
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr10:g.52815236G>C
GRCh37
chr10:g.54574996G>C
Linked Data - Sequence & Population
gnomAD v2:
10:54574996 G / C
gnomAD v3:
10:52815236 G / C
gnomAD v4:
chr10-52815236-G-C
Joint Max Group AF
0.85552944 (EAS)
Genomes Max Group AF
0.85552944 (EAS)
Linked Data - NCBI & NCI
dbSNP:
6480975
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000010.11:g.52815236G>C , CM000672.2:g.52815236G>C
GRCh38
NC_000010.10:g.54574996G>C , CM000672.1:g.54574996G>C
GRCh37
NC_000010.9:g.54245002G>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'