ClinGen Allele Registry
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Canonical Allele Identifier:
CA531013788
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr2:g.11897386_11897388del
GRCh37
chr2:g.12037512_12037514del
Linked Data - Sequence & Population
gnomAD v2:
2:12037511 CTTT / C
gnomAD v3:
2:11897385 CTTT / C
gnomAD v4:
chr2-11897385-CTTT-C
Linked Data - NCBI & NCI
dbSNP:
11292824
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000002.12:g.11897398_11897400del , CM000664.2:g.11897398_11897400del
GRCh38
NC_000002.11:g.12037524_12037526del , CM000664.1:g.12037524_12037526del
GRCh37
NC_000002.10:g.11954975_11954977del
NCBI36
Search 100 bp 5'
Search 100 bp 3'