Canonical Allele Identifier: CA51878367
Gene:

Linked Data

dbSNP Id: rs768606637
MyVariant Identifiers: chr2:g.88315870_88315871insTTAGCAGGTGCACCGTTTCTGGAAGTACTGCAATACCAAAT (hg19) chr2:g.88016351_88016352insTTAGCAGGTGCACCGTTTCTGGAAGTACTGCAATACCAAAT (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016352_88016392dup , CM000664.2:g.88016352_88016392dup GRCh38
NC_000002.11:g.88315871_88315911dup , CM000664.1:g.88315871_88315911dup GRCh37
NC_000002.10:g.88096986_88097026dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.697_737dup
XR_940336.3:n.697_737dup
Search 100 bp 5'
Search 100 bp 3'