ClinGen Allele Registry
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Canonical Allele Identifier:
CA175080025
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr8:g.33707860G>A
GRCh38
chr8:g.33707860_33707863delinsAGTA
GRCh37
chr8:g.33565378G>A
GRCh37
chr8:g.33565378_33565381delinsAGTA
Linked Data - Sequence & Population
gnomAD v2:
8:33565378 G / A
gnomAD v3:
8:33707860 G / A
gnomAD v4:
chr8-33707860-G-A
Joint Max Group AF
0.18953501 (EAS)
Genomes Max Group AF
0.18953501 (EAS)
Linked Data - NCBI & NCI
dbSNP:
4469412
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000008.11:g.33707860G>A , CM000670.2:g.33707860G>A
GRCh38
NC_000008.10:g.33565378G>A , CM000670.1:g.33565378G>A
GRCh37
NC_000008.9:g.33684920G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'