ClinGen Allele Registry
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Canonical Allele Identifier:
CA810626900
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr5:g.40414865_40414866insGTG
GRCh37
chr5:g.40414967_40414968insGTG
Linked Data - NCBI & NCI
dbSNP:
1254929296
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.40414867_40414868insGGT , CM000667.2:g.40414867_40414868insGGT
GRCh38
NC_000005.9:g.40414969_40414970insGGT , CM000667.1:g.40414969_40414970insGGT
GRCh37
NC_000005.8:g.40450726_40450727insGGT
NCBI36
Search 100 bp 5'
Search 100 bp 3'