Canonical Allele Identifier: CA2273427968
Gene: CASC17 HGNC NCBI

Linked Data

dbSNP Id: rs1907991276

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.71112762G>C , CM000679.2:g.71112762G>C GRCh38
NC_000017.10:g.69108903G>C , CM000679.1:g.69108903G>C GRCh37
NC_000017.9:g.66620498G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_104152.1:n.218-13144C>G