Canonical Allele Identifier: CA847168618
Gene: CASC8 HGNC NCBI

Linked Data

dbSNP Id: rs1278837513

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127473817T>C , CM000670.2:g.127473817T>C GRCh38
NC_000008.10:g.128486062T>C , CM000670.1:g.128486062T>C GRCh37
NC_000008.9:g.128555244T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_024393.1:n.1041+5266A>G
NR_117100.1:n.1041+5266A>G