Canonical Allele Identifier: CA185745480
Gene: CASC8 HGNC NCBI

Linked Data

dbSNP Id: rs1038321607

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127473686A>T , CM000670.2:g.127473686A>T GRCh38
NC_000008.10:g.128485931A>T , CM000670.1:g.128485931A>T GRCh37
NC_000008.9:g.128555113A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_024393.1:n.1041+5397T>A
NR_117100.1:n.1041+5397T>A