Canonical Allele Identifier: CA622658865

Gene: CASC16

Linked Data

• dbSNP Id: rs1379240015
• gnomAD v2: 16-52586353-A-G
• gnomAD v3: 16-52552441-A-G
• gnomAD v4: 16-52552441-A-G
• MyVariant Identifiers: chr16:g.52586353A>G (hg19) ; chr16:g.52552441A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.52552441A>G , CM000678.2:g.52552441A>G	GRCh38
NC_000016.9:g.52586353A>G , CM000678.1:g.52586353A>G	GRCh37
NC_000016.8:g.51143854A>G	NCBI36
NG_012623.1:g.362T>C

Transcript Alleles

HGVS	Amino-acid Change
NR_033920.1:n.654-7T>C