Canonical Allele Identifier: CA293056327
Gene: CASC17 HGNC NCBI

Linked Data

dbSNP Id: rs971321414
MyVariant Identifiers: chr17:g.71112590C>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.71112590C>G , CM000679.2:g.71112590C>G GRCh38
NC_000017.10:g.69108731C>G , CM000679.1:g.69108731C>G GRCh37
NC_000017.9:g.66620326C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_104152.1:n.218-12972G>C