Canonical Allele Identifier: CA185745383
Gene: CASC8 HGNC NCBI

Linked Data

dbSNP Id: rs897034483
MyVariant Identifiers: chr8:g.128485027G>A (hg19) chr8:g.127472782G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127472782G>A , CM000670.2:g.127472782G>A GRCh38
NC_000008.10:g.128485027G>A , CM000670.1:g.128485027G>A GRCh37
NC_000008.9:g.128554209G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_024393.1:n.1041+6301C>T
NR_117100.1:n.1041+6301C>T
Search 100 bp 5'
Search 100 bp 3'