Canonical Allele Identifier: CA666857959
Gene:

Linked Data

dbSNP Id: rs1306408349
gnomAD v3: 10-57812578-TC-T
gnomAD v4: 10-57812578-TC-T
MyVariant Identifiers: chr10:g.59572339del (hg19) chr10:g.57812579del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.57812580del , CM000672.2:g.57812580del GRCh38
NC_000010.10:g.59572340del , CM000672.1:g.59572340del GRCh37
NC_000010.9:g.59242346del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945979.1:n.68+34713del
XR_001747454.1:n.85+34713del
Search 100 bp 5'
Search 100 bp 3'