ClinGen Allele Registry
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Canonical Allele Identifier:
CA531013790
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr2:g.11897400_11897405delinsCAAACA
GRCh37
chr2:g.12037526_12037531delinsCAAACA
Linked Data - Sequence & Population
gnomAD v2:
2:12037526 T / C
gnomAD v3:
2:11897400 T / C
gnomAD v4:
chr2-11897400-T-C
Linked Data - NCBI & NCI
dbSNP:
868505680
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000002.12:g.11897400T>C , CM000664.2:g.11897400T>C
GRCh38
NC_000002.11:g.12037526T>C , CM000664.1:g.12037526T>C
GRCh37
NC_000002.10:g.11954977T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'