Canonical Allele Identifier: CA185745481

Gene: CASC8

Linked Data

• dbSNP Id: rs897078850
• gnomAD v2: 8-128485942-A-C
• gnomAD v3: 8-127473697-A-C
• gnomAD v4: 8-127473697-A-C
• MyVariant Identifiers: chr8:g.128485942A>C (hg19) ; chr8:g.127473697A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.127473697A>C , CM000670.2:g.127473697A>C	GRCh38
NC_000008.10:g.128485942A>C , CM000670.1:g.128485942A>C	GRCh37
NC_000008.9:g.128555124A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_024393.1:n.1041+5386T>G
NR_117100.1:n.1041+5386T>G