ClinGen Allele Registry
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Canonical Allele Identifier:
CA14123038
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr15:g.82059859C>A
GRCh37
chr15:g.82352200C>A
Linked Data - Sequence & Population
gnomAD v2:
15:82352200 C / A
gnomAD v3:
15:82059859 C / A
gnomAD v4:
chr15-82059859-C-A
Joint Max Group AF
0.85542673 (AFR)
Genomes Max Group AF
0.85542673 (AFR)
Linked Data - NCBI & NCI
dbSNP:
12324805
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000015.10:g.82059859C>A , CM000677.2:g.82059859C>A
GRCh38
NC_000015.9:g.82352200C>A , CM000677.1:g.82352200C>A
GRCh37
NC_000015.8:g.80139255C>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'