Canonical Allele Identifier: CA985992394
Gene: CASC17 HGNC NCBI

Linked Data

dbSNP Id: rs1908472948

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.71129511C>T , CM000679.2:g.71129511C>T GRCh38
NC_000017.10:g.69125652C>T , CM000679.1:g.69125652C>T GRCh37
NC_000017.9:g.66637247C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_104152.1:n.217+2879G>A