ClinGen Allele Registry
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Canonical Allele Identifier:
CA269278781
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr15:g.38219782C>G
GRCh37
chr15:g.38511983C>G
Linked Data - Sequence & Population
gnomAD v2:
15:38511983 C / G
gnomAD v3:
15:38219782 C / G
gnomAD v4:
chr15-38219782-C-G
Joint Max Group AF
0.15381862 (AMR)
Genomes Max Group AF
0.15381862 (AMR)
Linked Data - NCBI & NCI
dbSNP:
16966460
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000015.10:g.38219782C>G , CM000677.2:g.38219782C>G
GRCh38
NC_000015.9:g.38511983C>G , CM000677.1:g.38511983C>G
GRCh37
NC_000015.8:g.36299275C>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'