Canonical Allele Identifier: CA2273427788
Gene: CASC17 HGNC NCBI

Linked Data

dbSNP Id: rs1907980752

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.71112335G>T , CM000679.2:g.71112335G>T GRCh38
NC_000017.10:g.69108476G>T , CM000679.1:g.69108476G>T GRCh37
NC_000017.9:g.66620071G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_104152.1:n.218-12717C>A