Canonical Allele Identifier: CA293056161
Gene: CASC17 HGNC NCBI

Linked Data

dbSNP Id: rs902972500
MyVariant Identifiers: chr17:g.69108457T>C (hg19) chr17:g.71112316T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.71112316T>C , CM000679.2:g.71112316T>C GRCh38
NC_000017.10:g.69108457T>C , CM000679.1:g.69108457T>C GRCh37
NC_000017.9:g.66620052T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_104152.1:n.218-12698A>G
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