Canonical Allele Identifier: CA666858038
Gene:

Linked Data

dbSNP Id: rs1470255806
gnomAD v3: 10-57812844-A-AC
gnomAD v4: 10-57812844-A-AC
MyVariant Identifiers: chr10:g.59572604_59572605insC (hg19) chr10:g.57812844_57812845insC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.57812845dup , CM000672.2:g.57812845dup GRCh38
NC_000010.10:g.59572605dup , CM000672.1:g.59572605dup GRCh37
NC_000010.9:g.59242611dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945979.1:n.68+34447dup
XR_001747454.1:n.85+34447dup
Search 100 bp 5'
Search 100 bp 3'