ClinGen Allele Registry
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Canonical Allele Identifier:
CA755818566
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr2:g.11897401del
GRCh37
chr2:g.12037527del
Linked Data - Sequence & Population
gnomAD v3:
2:11897400 TA / T
gnomAD v4:
chr2-11897400-TA-T
Linked Data - NCBI & NCI
dbSNP:
1443113556
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000002.12:g.11897403del , CM000664.2:g.11897403del
GRCh38
NC_000002.11:g.12037529del , CM000664.1:g.12037529del
GRCh37
NC_000002.10:g.11954980del
NCBI36
Search 100 bp 5'
Search 100 bp 3'