ClinGen Allele Registry
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Canonical Allele Identifier:
CA14149353
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr15:g.79138721A>G
GRCh37
chr15:g.79431063A>G
Linked Data - Sequence & Population
gnomAD v2:
15:79431063 A / G
gnomAD v3:
15:79138721 A / G
gnomAD v4:
chr15-79138721-A-G
Joint Max Group AF
0.6607422 (SAS)
Genomes Max Group AF
0.6607422 (SAS)
Linked Data - NCBI & NCI
dbSNP:
939661
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000015.10:g.79138721A>G , CM000677.2:g.79138721A>G
GRCh38
NC_000015.9:g.79431063A>G , CM000677.1:g.79431063A>G
GRCh37
NC_000015.8:g.77218118A>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'