ClinGen Allele Registry
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Canonical Allele Identifier:
CA202300546
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr10:g.5995763C>T
GRCh37
chr10:g.6037726C>T
Linked Data - Sequence & Population
gnomAD v2:
10:6037726 C / T
gnomAD v3:
10:5995763 C / T
gnomAD v4:
chr10-5995763-C-T
Joint Max Group AF
0.12953016 (MID)
Genomes Max Group AF
0.11400664 (NFE)
Linked Data - NCBI & NCI
dbSNP:
7911500
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000010.11:g.5995763C>T , CM000672.2:g.5995763C>T
GRCh38
NC_000010.10:g.6037726C>T , CM000672.1:g.6037726C>T
GRCh37
NC_000010.9:g.6077732C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'