Canonical Allele Identifier: CA853716196
Gene:

Linked Data

dbSNP Id: rs1378303482
MyVariant Identifiers: chr8:g.5765325_5765328del (hg19) chr8:g.5907803_5907806del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.5907807_5907810del , CM000670.2:g.5907807_5907810del GRCh38
NC_000008.10:g.5765329_5765332del , CM000670.1:g.5765329_5765332del GRCh37
NC_000008.9:g.5752737_5752740del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_941374.1:n.308-8075_308-8072del
XR_941375.1:n.308-8075_308-8072del
XR_941376.1:n.406-8075_406-8072del
XR_941377.1:n.308-8075_308-8072del
XR_941378.1:n.216-8075_216-8072del
XR_001745765.1:n.308-8075_308-8072del
XR_001745766.1:n.406-8075_406-8072del
XR_001745767.1:n.216-8075_216-8072del
XR_001745768.1:n.308-8075_308-8072del
XR_941374.2:n.308-8075_308-8072del
XR_941375.2:n.308-8075_308-8072del
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