ClinGen Allele Registry
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Canonical Allele Identifier:
CA212844606
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr10:g.99781858C>A
GRCh37
chr10:g.101541615C>A
Linked Data - Sequence & Population
gnomAD v2:
10:101541615 C / A
gnomAD v3:
10:99781858 C / A
gnomAD v4:
chr10-99781858-C-A
Joint Max Group AF
0.00006271 (AFR)
Genomes Max Group AF
0.00006271 (AFR)
Linked Data - NCBI & NCI
dbSNP:
540452611
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000010.11:g.99781858C>A , CM000672.2:g.99781858C>A
GRCh38
NC_000010.10:g.101541615C>A , CM000672.1:g.101541615C>A
GRCh37
NC_000010.9:g.101531605C>A
NCBI36
NG_011798.1:g.4153C>A
NG_011798.2:g.4261C>A
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