Canonical Allele Identifier: CA293056363
Gene: CASC17 HGNC NCBI

Linked Data

dbSNP Id: rs1054591779

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.71112654T>C , CM000679.2:g.71112654T>C GRCh38
NC_000017.10:g.69108795T>C , CM000679.1:g.69108795T>C GRCh37
NC_000017.9:g.66620390T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_104152.1:n.218-13036A>G