Canonical Allele Identifier: CA1818375137
Gene: CASC8 HGNC NCBI

Linked Data

dbSNP Id: rs1815898493

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127473692G>T , CM000670.2:g.127473692G>T GRCh38
NC_000008.10:g.128485937G>T , CM000670.1:g.128485937G>T GRCh37
NC_000008.9:g.128555119G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_024393.1:n.1041+5391C>A
NR_117100.1:n.1041+5391C>A