ClinGen Allele Registry
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Canonical Allele Identifier:
CA215016596
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr10:g.117467831G>T
GRCh37
chr10:g.119227342G>T
Linked Data - Sequence & Population
gnomAD v2:
10:119227342 G / T
gnomAD v3:
10:117467831 G / T
gnomAD v4:
chr10-117467831-G-T
Joint Max Group AF
0.09975072 (MID)
Genomes Max Group AF
0.08627714 (SAS)
Linked Data - NCBI & NCI
dbSNP:
4752066
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000010.11:g.117467831G>T , CM000672.2:g.117467831G>T
GRCh38
NC_000010.10:g.119227342G>T , CM000672.1:g.119227342G>T
GRCh37
NC_000010.9:g.119217332G>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'