Canonical Allele Identifier: CA627480396
Gene: CASC17 HGNC NCBI

Linked Data

dbSNP Id: rs1429906030

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.71112709A>C , CM000679.2:g.71112709A>C GRCh38
NC_000017.10:g.69108850A>C , CM000679.1:g.69108850A>C GRCh37
NC_000017.9:g.66620445A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_104152.1:n.218-13091T>G