Canonical Allele Identifier: CA51878382
Gene:

Linked Data

dbSNP Id: rs1553449782
MyVariant Identifiers: chr2:g.88315911_88315912insCTGTTTTTGTCACTAATGG (hg19) chr2:g.88016392_88016393insCTGTTTTTGTCACTAATGG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016393_88016394insTGTTTTTGTCACTAATGGC , CM000664.2:g.88016393_88016394insTGTTTTTGTCACTAATGGC GRCh38
NC_000002.11:g.88315912_88315913insTGTTTTTGTCACTAATGGC , CM000664.1:g.88315912_88315913insTGTTTTTGTCACTAATGGC GRCh37
NC_000002.10:g.88097027_88097028insTGTTTTTGTCACTAATGGC NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.738_739insTGTTTTTGTCACTAATGGC
XR_940336.3:n.738_739insTGTTTTTGTCACTAATGGC
Search 100 bp 5'
Search 100 bp 3'