ClinGen Allele Registry
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Canonical Allele Identifier:
CA15847825
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr15:g.69755818A>C
GRCh37
chr15:g.70048157A>C
Linked Data - Sequence & Population
gnomAD v2:
15:70048157 A / C
gnomAD v3:
15:69755818 A / C
gnomAD v4:
chr15-69755818-A-C
Joint Max Group AF
0.12925203 (AFR)
Genomes Max Group AF
0.12925203 (AFR)
Linked Data - NCBI & NCI
dbSNP:
10152591
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000015.10:g.69755818A>C , CM000677.2:g.69755818A>C
GRCh38
NC_000015.9:g.70048157A>C , CM000677.1:g.70048157A>C
GRCh37
NC_000015.8:g.67835211A>C
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
XR_001751592.2:n.86-338A>C
Search 100 bp 5'
Search 100 bp 3'