Canonical Allele Identifier: CA185745367
Gene: CASC8 HGNC NCBI

Linked Data

dbSNP Id: rs893911455

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127472677G>C , CM000670.2:g.127472677G>C GRCh38
NC_000008.10:g.128484922G>C , CM000670.1:g.128484922G>C GRCh37
NC_000008.9:g.128554104G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_024393.1:n.1041+6406C>G
NR_117100.1:n.1041+6406C>G