ClinGen Allele Registry
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Canonical Allele Identifier:
CA11229499
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr2:g.82802345C>G
GRCh37
chr2:g.83029469C>G
Linked Data - Sequence & Population
gnomAD v2:
2:83029469 C / G
gnomAD v3:
2:82802345 C / G
gnomAD v4:
chr2-82802345-C-G
Joint Max Group AF
0.04377608 (AFR)
Genomes Max Group AF
0.04377608 (AFR)
Linked Data - NCBI & NCI
dbSNP:
17022444
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000002.12:g.82802345C>G , CM000664.2:g.82802345C>G
GRCh38
NC_000002.11:g.83029469C>G , CM000664.1:g.83029469C>G
GRCh37
NC_000002.10:g.82882980C>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'