ClinGen Allele Registry
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Canonical Allele Identifier:
CA13822363
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr13:g.105370372A>G
GRCh37
chr13:g.106022722A>G
Linked Data - Sequence & Population
gnomAD v2:
13:106022722 A / G
gnomAD v3:
13:105370372 A / G
gnomAD v4:
chr13-105370372-A-G
Joint Max Group AF
0.15979892 (AFR)
Genomes Max Group AF
0.15979892 (AFR)
Linked Data - NCBI & NCI
dbSNP:
1535989
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000013.11:g.105370372A>G , CM000675.2:g.105370372A>G
GRCh38
NC_000013.10:g.106022722A>G , CM000675.1:g.106022722A>G
GRCh37
NC_000013.9:g.104820723A>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'