Canonical Allele Identifier: CA847190369
Gene: CASC11 HGNC NCBI

Linked Data

dbSNP Id: rs1174181685
MyVariant Identifiers: chr8:g.128718086_128718087insATT (hg19) chr8:g.127705841_127705842insATT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127705854_127705856dup , CM000670.2:g.127705854_127705856dup GRCh38
NC_000008.10:g.128718099_128718101dup , CM000670.1:g.128718099_128718101dup GRCh37
NC_000008.9:g.128787281_128787283dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_117102.1:n.366-2601_366-2599dup
Search 100 bp 5'
Search 100 bp 3'