ClinGen Allele Registry
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Canonical Allele Identifier:
CA13815781
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr13:g.70272071G>A
GRCh37
chr13:g.70846203G>A
Linked Data - Sequence & Population
gnomAD v2:
13:70846203 G / A
gnomAD v3:
13:70272071 G / A
gnomAD v4:
chr13-70272071-G-A
Joint Max Group AF
0.47716079 (EAS)
Genomes Max Group AF
0.47716079 (EAS)
Linked Data - NCBI & NCI
dbSNP:
9572423
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000013.11:g.70272071G>A , CM000675.2:g.70272071G>A
GRCh38
NC_000013.10:g.70846203G>A , CM000675.1:g.70846203G>A
GRCh37
NC_000013.9:g.69744204G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'