Canonical Allele Identifier: CA281875500

Gene: CASC16

Linked Data

• dbSNP Id: rs564101787
• gnomAD v2: 16-52586394-C-A
• gnomAD v3: 16-52552482-C-A
• gnomAD v4: 16-52552482-C-A
• MyVariant Identifiers: chr16:g.52586394C>A (hg19) ; chr16:g.52552482C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.52552482C>A , CM000678.2:g.52552482C>A	GRCh38
NC_000016.9:g.52586394C>A , CM000678.1:g.52586394C>A	GRCh37
NC_000016.8:g.51143895C>A	NCBI36
NG_012623.1:g.321G>T

Transcript Alleles

HGVS	Amino-acid Change
NR_033920.1:n.654-48G>T