Canonical Allele Identifier: CA847166739
Gene: CASC8 HGNC NCBI

Linked Data

dbSNP Id: rs562518007

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127472660C>A , CM000670.2:g.127472660C>A GRCh38
NC_000008.10:g.128484905C>A , CM000670.1:g.128484905C>A GRCh37
NC_000008.9:g.128554087C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_024393.1:n.1041+6423G>T
NR_117100.1:n.1041+6423G>T