ClinGen Allele Registry
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Canonical Allele Identifier:
CA13853697
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr13:g.113105440A>G
GRCh37
chr13:g.113759754A>G
Linked Data - Sequence & Population
gnomAD v2:
13:113759754 A / G
gnomAD v3:
13:113105440 A / G
gnomAD v4:
chr13-113105440-A-G
Joint Max Group AF
0.85503132 (AFR)
Genomes Max Group AF
0.85503132 (AFR)
Linked Data - NCBI & NCI
dbSNP:
510317
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000013.11:g.113105440A>G , CM000675.2:g.113105440A>G
GRCh38
NC_000013.10:g.113759754A>G , CM000675.1:g.113759754A>G
GRCh37
NC_000013.9:g.112807755A>G
NCBI36
NG_009262.1:g.4650A>G , LRG_554:g.4650A>G
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