Canonical Allele Identifier: CA185745385
Gene: CASC8 HGNC NCBI

Linked Data

dbSNP Id: rs972863616

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127472804A>G , CM000670.2:g.127472804A>G GRCh38
NC_000008.10:g.128485049A>G , CM000670.1:g.128485049A>G GRCh37
NC_000008.9:g.128554231A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_024393.1:n.1041+6279T>C
NR_117100.1:n.1041+6279T>C