ClinGen Allele Registry
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Canonical Allele Identifier:
CA11037419
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr2:g.170684313A>C
GRCh37
chr2:g.171540823A>C
Linked Data - Sequence & Population
gnomAD v2:
2:171540823 A / C
gnomAD v3:
2:170684313 A / C
gnomAD v4:
chr2-170684313-A-C
Joint Max Group AF
0.49841165 (AMR)
Genomes Max Group AF
0.49841165 (AMR)
Linked Data - NCBI & NCI
dbSNP:
2080401
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000002.12:g.170684313A>C , CM000664.2:g.170684313A>C
GRCh38
NC_000002.11:g.171540823A>C , CM000664.1:g.171540823A>C
GRCh37
NC_000002.10:g.171249069A>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'