ClinGen Allele Registry
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Canonical Allele Identifier:
CA269339735
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr15:g.38856422A>G
GRCh37
chr15:g.39148623A>G
Linked Data - Sequence & Population
gnomAD v2:
15:39148623 A / G
gnomAD v3:
15:38856422 A / G
gnomAD v4:
chr15-38856422-A-G
Joint Max Group AF
0.0000789 (AFR)
Genomes Max Group AF
0.0000789 (AFR)
Linked Data - NCBI & NCI
dbSNP:
1012009529
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000015.10:g.38856422A>G , CM000677.2:g.38856422A>G
GRCh38
NC_000015.9:g.39148623A>G , CM000677.1:g.39148623A>G
GRCh37
NC_000015.8:g.36935915A>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'