ClinGen Allele Registry
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Canonical Allele Identifier:
CA12909188
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr8:g.139507274G>T
GRCh38
chr8:g.139507274_139507278delinsTTGCT
GRCh37
chr8:g.140519517G>T
GRCh37
chr8:g.140519517_140519521delinsTTGCT
Linked Data - Sequence & Population
gnomAD v2:
8:140519517 G / T
gnomAD v3:
8:139507274 G / T
gnomAD v4:
chr8-139507274-G-T
Joint Max Group AF
0.73429142 (EAS)
Genomes Max Group AF
0.73429142 (EAS)
Linked Data - NCBI & NCI
dbSNP:
2468677
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000008.11:g.139507274G>T , CM000670.2:g.139507274G>T
GRCh38
NC_000008.10:g.140519517G>T , CM000670.1:g.140519517G>T
GRCh37
NC_000008.9:g.140588699G>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'