ClinGen Allele Registry
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Canonical Allele Identifier:
CA269319209
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr15:g.38703290A>G
GRCh37
chr15:g.38995491A>G
Linked Data - Sequence & Population
gnomAD v2:
15:38995491 A / G
gnomAD v3:
15:38703290 A / G
gnomAD v4:
chr15-38703290-A-G
Joint Max Group AF
0.28490543 (NFE)
Genomes Max Group AF
0.28490543 (NFE)
Linked Data - NCBI & NCI
dbSNP:
12899449
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000015.10:g.38703290A>G , CM000677.2:g.38703290A>G
GRCh38
NC_000015.9:g.38995491A>G , CM000677.1:g.38995491A>G
GRCh37
NC_000015.8:g.36782783A>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'