ClinGen Allele Registry
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Canonical Allele Identifier:
CA15846248
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr15:g.89358801A>C
GRCh37
chr15:g.89902032A>C
Linked Data - Sequence & Population
gnomAD v2:
15:89902032 A / C
gnomAD v3:
15:89358801 A / C
gnomAD v4:
chr15-89358801-A-C
Joint Max Group AF
0.79863377 (AFR)
Genomes Max Group AF
0.79863377 (AFR)
Exomes Max Group AF
0.23271423 (NFE)
Linked Data - NCBI & NCI
dbSNP:
4932217
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000015.10:g.89358801A>C , CM000677.2:g.89358801A>C
GRCh38
NC_000015.9:g.89902032A>C , CM000677.1:g.89902032A>C
GRCh37
NC_000015.8:g.87703036A>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'