Canonical Allele Identifier: CA185745499
Gene: CASC8 HGNC NCBI

Linked Data

dbSNP Id: rs998730045

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127473798C>T , CM000670.2:g.127473798C>T GRCh38
NC_000008.10:g.128486043C>T , CM000670.1:g.128486043C>T GRCh37
NC_000008.9:g.128555225C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_024393.1:n.1041+5285G>A
NR_117100.1:n.1041+5285G>A