ClinGen Allele Registry
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Canonical Allele Identifier:
CA729425882
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.193656103G>T
GRCh37
chr1:g.193625233G>T
Linked Data - Sequence & Population
gnomAD v3:
1:193656103 G / T
gnomAD v4:
chr1-193656103-G-T
Joint Max Group AF
0.00005295 (AMR)
Genomes Max Group AF
0.00005295 (AMR)
Linked Data - NCBI & NCI
dbSNP:
6678275
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.193656103G>T , CM000663.2:g.193656103G>T
GRCh38
NC_000001.10:g.193625233G>T , CM000663.1:g.193625233G>T
GRCh37
NC_000001.9:g.191891856G>T
NCBI36
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