ClinGen Allele Registry
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Canonical Allele Identifier:
CA269178763
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr15:g.37356201A>C
GRCh37
chr15:g.37648402A>C
Linked Data - Sequence & Population
gnomAD v2:
15:37648402 A / C
gnomAD v3:
15:37356201 A / C
gnomAD v4:
chr15-37356201-A-C
Joint Max Group AF
0.61843783 (EAS)
Genomes Max Group AF
0.61843783 (EAS)
Linked Data - NCBI & NCI
dbSNP:
8025231
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000015.10:g.37356201A>C , CM000677.2:g.37356201A>C
GRCh38
NC_000015.9:g.37648402A>C , CM000677.1:g.37648402A>C
GRCh37
NC_000015.8:g.35435694A>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'