Canonical Allele Identifier: CA775632394
Gene:

Linked Data

dbSNP Id: rs1461050856
MyVariant Identifiers: chr17:g.8040996_8040997insGAAG (hg19) chr17:g.8137678_8137679insGAAG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8137682_8137685dup , CM000679.2:g.8137682_8137685dup GRCh38
NC_000017.10:g.8041000_8041003dup , CM000679.1:g.8041000_8041003dup GRCh37
NC_000017.9:g.7981725_7981728dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_934202.1:n.183-1167_183-1164dup
XR_934203.1:n.70-1795_70-1792dup
XR_934202.2:n.414-1167_414-1164dup
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