Canonical Allele Identifier: CA185745487
Gene: CASC8 HGNC NCBI

Linked Data

dbSNP Id: rs1043903610

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127473736A>G , CM000670.2:g.127473736A>G GRCh38
NC_000008.10:g.128485981A>G , CM000670.1:g.128485981A>G GRCh37
NC_000008.9:g.128555163A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_024393.1:n.1041+5347T>C
NR_117100.1:n.1041+5347T>C