Canonical Allele Identifier: CA1818373899
Gene: CASC8 HGNC NCBI

Linked Data

dbSNP Id: rs1815885941

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127472730T>C , CM000670.2:g.127472730T>C GRCh38
NC_000008.10:g.128484975T>C , CM000670.1:g.128484975T>C GRCh37
NC_000008.9:g.128554157T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_024393.1:n.1041+6353A>G
NR_117100.1:n.1041+6353A>G