Canonical Allele Identifier: CA495704406

Gene: CASC16

Linked Data

• dbSNP Id: rs1218041254
• gnomAD v3: 16-52552374-A-G
• gnomAD v4: 16-52552374-A-G
• MyVariant Identifiers: chr16:g.52586286A>G (hg19) ; chr16:g.52552374A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.52552374A>G , CM000678.2:g.52552374A>G	GRCh38
NC_000016.9:g.52586286A>G , CM000678.1:g.52586286A>G	GRCh37
NC_000016.8:g.51143787A>G	NCBI36
NG_012623.1:g.429T>C

Transcript Alleles

HGVS	Amino-acid change
NR_033920.1:n.714T>C