ClinGen Allele Registry
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Canonical Allele Identifier:
CA15849327
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr15:g.57589691T>G
GRCh37
chr15:g.57881889T>G
Linked Data - Sequence & Population
gnomAD v2:
15:57881889 T / G
gnomAD v3:
15:57589691 T / G
gnomAD v4:
chr15-57589691-T-G
Joint Max Group AF
0.90490986 (EAS)
Genomes Max Group AF
0.90490986 (EAS)
Linked Data - NCBI & NCI
dbSNP:
744318
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000015.10:g.57589691T>G , CM000677.2:g.57589691T>G
GRCh38
NC_000015.9:g.57881889T>G , CM000677.1:g.57881889T>G
GRCh37
NC_000015.8:g.55669181T>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'