ClinGen Allele Registry
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Canonical Allele Identifier:
CA755818553
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr2:g.11897385_11897386insTT
GRCh37
chr2:g.12037511_12037512insTT
Linked Data - Sequence & Population
gnomAD v3:
2:11897385 C / CTT
gnomAD v4:
chr2-11897385-C-CTT
Linked Data - NCBI & NCI
dbSNP:
11292824
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000002.12:g.11897399_11897400dup , CM000664.2:g.11897399_11897400dup
GRCh38
NC_000002.11:g.12037525_12037526dup , CM000664.1:g.12037525_12037526dup
GRCh37
NC_000002.10:g.11954976_11954977dup
NCBI36
Search 100 bp 5'
Search 100 bp 3'