Canonical Allele Identifier: CA2963855259
Gene: CASC17 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.71112615T>C , CM000679.2:g.71112615T>C GRCh38
NC_000017.10:g.69108756T>C , CM000679.1:g.69108756T>C GRCh37
NC_000017.9:g.66620351T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_104152.1:n.218-12997A>G