Canonical Allele Identifier: CA1119004206
Gene: CASC8 HGNC NCBI

Linked Data

dbSNP Id: rs1815886897

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127472794G>A , CM000670.2:g.127472794G>A GRCh38
NC_000008.10:g.128485039G>A , CM000670.1:g.128485039G>A GRCh37
NC_000008.9:g.128554221G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_024393.1:n.1041+6289C>T
NR_117100.1:n.1041+6289C>T