Canonical Allele Identifier: CA775632204
Gene:

Linked Data

dbSNP Id: rs1323020398
MyVariant Identifiers: chr17:g.8040565_8040568del (hg19) chr17:g.8137247_8137250del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8137248_8137251del , CM000679.2:g.8137248_8137251del GRCh38
NC_000017.10:g.8040566_8040569del , CM000679.1:g.8040566_8040569del GRCh37
NC_000017.9:g.7981291_7981294del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_934202.1:n.183-1601_183-1598del
XR_934203.1:n.70-2229_70-2226del
XR_934202.2:n.414-1601_414-1598del
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