Canonical Allele Identifier: CA293056179
Gene: CASC17 HGNC NCBI

Linked Data

dbSNP Id: rs760477008
MyVariant Identifiers: chr17:g.69108477del (hg19) chr17:g.71112336del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.71112338del , CM000679.2:g.71112338del GRCh38
NC_000017.10:g.69108479del , CM000679.1:g.69108479del GRCh37
NC_000017.9:g.66620074del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_104152.1:n.218-12718del
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