Canonical Allele Identifier: CA281877258

Gene: CASC16

Linked Data

• dbSNP Id: rs3112571
• gnomAD v2: 16-52601111-C-A
• gnomAD v3: 16-52567199-C-A
• gnomAD v4: 16-52567199-C-A
• MyVariant Identifiers: chr16:g.52601111C>A (hg19) ; chr16:g.52567199C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.52567199C>A , CM000678.2:g.52567199C>A	GRCh38
NC_000016.9:g.52601111C>A , CM000678.1:g.52601111C>A	GRCh37
NC_000016.8:g.51158612C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_033920.1:n.605-4337G>T