Canonical Allele Identifier: CA281877269

Gene: CASC16

Linked Data

• dbSNP Id: rs1014669567
• gnomAD v2: 16-52601219-G-C
• gnomAD v3: 16-52567307-G-C
• gnomAD v4: 16-52567307-G-C
• MyVariant Identifiers: chr16:g.52601219G>C (hg19) ; chr16:g.52567307G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.52567307G>C , CM000678.2:g.52567307G>C	GRCh38
NC_000016.9:g.52601219G>C , CM000678.1:g.52601219G>C	GRCh37
NC_000016.8:g.51158720G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_033920.1:n.605-4445C>G