Canonical Allele Identifier: CA1818373859
Gene: CASC8 HGNC NCBI

Linked Data

dbSNP Id: rs1815885621

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127472714C>T , CM000670.2:g.127472714C>T GRCh38
NC_000008.10:g.128484959C>T , CM000670.1:g.128484959C>T GRCh37
NC_000008.9:g.128554141C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_024393.1:n.1041+6369G>A
NR_117100.1:n.1041+6369G>A