Canonical Allele Identifier: CA495703671

Gene: CASC16

Linked Data

• dbSNP Id: rs1434901204
• gnomAD v3: 16-52552246-C-A
• gnomAD v4: 16-52552246-C-A
• MyVariant Identifiers: chr16:g.52586158C>A (hg19) ; chr16:g.52552246C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.52552246C>A , CM000678.2:g.52552246C>A	GRCh38
NC_000016.9:g.52586158C>A , CM000678.1:g.52586158C>A	GRCh37
NC_000016.8:g.51143659C>A	NCBI36
NG_012623.1:g.557G>T

Transcript Alleles

HGVS	Amino-acid change
NR_033920.1:n.842G>T