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Canonical Allele Identifier:
CA865471349
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr9:g.6365625_6365635del
GRCh37
chr9:g.6365625_6365635del
Linked Data - NCBI & NCI
dbSNP:
1455601344
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.6365628_6365638del , CM000671.2:g.6365628_6365638del
GRCh38
NC_000009.11:g.6365628_6365638del , CM000671.1:g.6365628_6365638del
GRCh37
NC_000009.10:g.6355628_6355638del
NCBI36
Search 100 bp 5'
Search 100 bp 3'