Canonical Allele Identifier: CA51878235
Gene:

Linked Data

dbSNP Id: rs994077002
MyVariant Identifiers: chr2:g.88315414_88315415insCCCAAAT (hg19) chr2:g.88015895_88015896insCCCAAAT (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88015900_88015906dup , CM000664.2:g.88015900_88015906dup GRCh38
NC_000002.11:g.88315419_88315425dup , CM000664.1:g.88315419_88315425dup GRCh37
NC_000002.10:g.88096534_88096540dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.245_251dup
XR_940336.3:n.245_251dup
Search 100 bp 5'
Search 100 bp 3'