ClinGen Allele Registry
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Canonical Allele Identifier:
CA15666852
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr10:g.95069673G>T
GRCh37
chr10:g.96829430G>T
Linked Data - Sequence & Population
gnomAD v2:
10:96829430 G / T
gnomAD v3:
10:95069673 G / T
gnomAD v4:
chr10-95069673-G-T
Joint Max Group AF
0.247517 (AMR)
Genomes Max Group AF
0.247517 (AMR)
Linked Data - NCBI & NCI
dbSNP:
7909236
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000010.11:g.95069673G>T , CM000672.2:g.95069673G>T
GRCh38
NC_000010.10:g.96829430G>T , CM000672.1:g.96829430G>T
GRCh37
NC_000010.9:g.96819420G>T
NCBI36
NG_007972.1:g.4825C>A
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