Canonical Allele Identifier: CA894254852
Gene:

Linked Data

dbSNP Id: rs1420138601
MyVariant Identifiers: chr2:g.88315895del (hg19) chr2:g.88016376del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016376del , CM000664.2:g.88016376del GRCh38
NC_000002.11:g.88315895del , CM000664.1:g.88315895del GRCh37
NC_000002.10:g.88097010del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.721del
XR_940336.3:n.721del
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