ClinGen Allele Registry
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Canonical Allele Identifier:
CA54680808
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr2:g.120487456del
GRCh37
chr2:g.121245032del
Linked Data - Sequence & Population
gnomAD v2:
2:121245031 CG / C
gnomAD v3:
2:120487455 CG / C
gnomAD v4:
chr2-120487455-CG-C
Joint Max Group AF
0.00762604 (AFR)
Genomes Max Group AF
0.00762604 (AFR)
Linked Data - NCBI & NCI
dbSNP:
578185535
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000002.12:g.120487459del , CM000664.2:g.120487459del
GRCh38
NC_000002.11:g.121245035del , CM000664.1:g.121245035del
GRCh37
NC_000002.10:g.120961505del
NCBI36
Search 100 bp 5'
Search 100 bp 3'