Canonical Allele Identifier: CA2718189994
Gene: CASC8 HGNC NCBI

Linked Data

dbSNP Id: rs2129708638

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127473733G>T , CM000670.2:g.127473733G>T GRCh38
NC_000008.10:g.128485978G>T , CM000670.1:g.128485978G>T GRCh37
NC_000008.9:g.128555160G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_024393.1:n.1041+5350C>A
NR_117100.1:n.1041+5350C>A