Canonical Allele Identifier: CA856539075
Gene:

Linked Data

dbSNP Id: rs1359150887
gnomAD v3: 8-88535772-GA-G
gnomAD v4: 8-88535772-GA-G
MyVariant Identifiers: chr8:g.89548002del (hg19) chr8:g.88535773del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.88535773del , CM000670.2:g.88535773del GRCh38
NC_000008.10:g.89548002del , CM000670.1:g.89548002del GRCh37
NC_000008.9:g.89617118del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001745651.2:n.1673+10744del
XR_001745653.2:n.286-6907del
XR_928383.3:n.1475+10744del
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