ClinGen Allele Registry
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Canonical Allele Identifier:
CA11131004
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr2:g.165034223A>C
GRCh37
chr2:g.165890733A>C
Linked Data - Sequence & Population
gnomAD v2:
2:165890733 A / C
gnomAD v3:
2:165034223 A / C
gnomAD v4:
chr2-165034223-A-C
Joint Max Group AF
0.35022281 (NFE)
Genomes Max Group AF
0.35022281 (NFE)
Linked Data - NCBI & NCI
dbSNP:
776488
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000002.12:g.165034223A>C , CM000664.2:g.165034223A>C
GRCh38
NC_000002.11:g.165890733A>C , CM000664.1:g.165890733A>C
GRCh37
NC_000002.10:g.165598979A>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'