ClinGen Allele Registry
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Canonical Allele Identifier:
CA14105014
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr15:g.67810868G>C
GRCh37
chr15:g.68103206G>C
Linked Data - Sequence & Population
gnomAD v2:
15:68103206 G / C
gnomAD v3:
15:67810868 G / C
gnomAD v4:
chr15-67810868-G-C
Joint Max Group AF
0.6785389 (EAS)
Genomes Max Group AF
0.6785389 (EAS)
Linked Data - NCBI & NCI
dbSNP:
6494696
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000015.10:g.67810868G>C , CM000677.2:g.67810868G>C
GRCh38
NC_000015.9:g.68103206G>C , CM000677.1:g.68103206G>C
GRCh37
NC_000015.8:g.65890260G>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'