ClinGen Allele Registry
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Canonical Allele Identifier:
CA15700990
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr11:g.130053128T>A
GRCh37
chr11:g.129923023T>A
Linked Data - Sequence & Population
gnomAD v2:
11:129923023 T / A
gnomAD v3:
11:130053128 T / A
gnomAD v4:
chr11-130053128-T-A
Joint Max Group AF
0.07894017 (AFR)
Genomes Max Group AF
0.07894017 (AFR)
Linked Data - NCBI & NCI
dbSNP:
7127037
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.130053128T>A , CM000673.2:g.130053128T>A
GRCh38
NC_000011.9:g.129923023T>A , CM000673.1:g.129923023T>A
GRCh37
NC_000011.8:g.129428233T>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'