Canonical Allele Identifier: CA894254718
Gene:

Linked Data

dbSNP Id: rs1440202470
MyVariant Identifiers: chr2:g.88315869_88315909del (hg19) chr2:g.88016350_88016390del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016350_88016390del , CM000664.2:g.88016350_88016390del GRCh38
NC_000002.11:g.88315869_88315909del , CM000664.1:g.88315869_88315909del GRCh37
NC_000002.10:g.88096984_88097024del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.695_735del
XR_940336.3:n.695_735del
Search 100 bp 5'
Search 100 bp 3'