Canonical Allele Identifier: CA802056765
Gene:

Linked Data

ClinVar Variation Id: 1059614
ClinVar RCV Id: RCV003538757
dbSNP Id: rs1329132451
MyVariant Identifiers: chr5:g.112043009_112043010insTGCA (hg19) chr5:g.112707312_112707313insTGCA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112707313_112707316dup , CM000667.2:g.112707313_112707316dup GRCh38
NC_000005.9:g.112043010_112043013dup , CM000667.1:g.112043010_112043013dup GRCh37
NC_000005.8:g.112070909_112070912dup NCBI36
NG_008481.4:g.19793_19796dup , LRG_130:g.19793_19796dup
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