ClinGen Allele Registry
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Canonical Allele Identifier:
CA15856562
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr15:g.95613139A>G
GRCh37
chr15:g.96156368A>G
Linked Data - Sequence & Population
gnomAD v2:
15:96156368 A / G
gnomAD v3:
15:95613139 A / G
gnomAD v4:
chr15-95613139-A-G
Joint Max Group AF
0.32888347 (AFR)
Genomes Max Group AF
0.32888347 (AFR)
Linked Data - NCBI & NCI
dbSNP:
4321143
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000015.10:g.95613139A>G , CM000677.2:g.95613139A>G
GRCh38
NC_000015.9:g.96156368A>G , CM000677.1:g.96156368A>G
GRCh37
NC_000015.8:g.93957372A>G
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
XR_932654.1:n.68+3063A>G
Search 100 bp 5'
Search 100 bp 3'