Canonical Allele Identifier: CA774666438
Gene: CASC17 HGNC NCBI

Linked Data

dbSNP Id: rs1442777934
MyVariant Identifiers: chr17:g.69108889C>A (hg19) chr17:g.71112748C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.71112748C>A , CM000679.2:g.71112748C>A GRCh38
NC_000017.10:g.69108889C>A , CM000679.1:g.69108889C>A GRCh37
NC_000017.9:g.66620484C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_104152.1:n.218-13130G>T
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