ClinGen Allele Registry
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Canonical Allele Identifier:
CA728695982
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.186681564G>T
GRCh37
chr1:g.186650696G>T
Linked Data - Sequence & Population
gnomAD v3:
1:186681564 G / T
gnomAD v4:
chr1-186681564-G-T
Joint Max Group AF
0.00001922 (AFR)
Genomes Max Group AF
0.00001922 (AFR)
Linked Data - NCBI & NCI
dbSNP:
1226172087
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.186681564G>T , CM000663.2:g.186681564G>T
GRCh38
NC_000001.10:g.186650696G>T , CM000663.1:g.186650696G>T
GRCh37
NC_000001.9:g.184917319G>T
NCBI36
NG_028206.2:g.3864C>A
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