Canonical Allele Identifier: CA293056422
Gene: CASC17 HGNC NCBI

Linked Data

dbSNP Id: rs923433595

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.71112768T>C , CM000679.2:g.71112768T>C GRCh38
NC_000017.10:g.69108909T>C , CM000679.1:g.69108909T>C GRCh37
NC_000017.9:g.66620504T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_104152.1:n.218-13150A>G