Canonical Allele Identifier: CA2273427923
Gene: CASC17 HGNC NCBI

Linked Data

dbSNP Id: rs1907988783

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.71112658T>C , CM000679.2:g.71112658T>C GRCh38
NC_000017.10:g.69108799T>C , CM000679.1:g.69108799T>C GRCh37
NC_000017.9:g.66620394T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_104152.1:n.218-13040A>G