Canonical Allele Identifier: CA495704309

Gene: CASC16

Linked Data

• dbSNP Id: rs1219044392
• gnomAD v4: 16-52552358-T-C
• MyVariant Identifiers: chr16:g.52586270T>C (hg19) ; chr16:g.52552358T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.52552358T>C , CM000678.2:g.52552358T>C	GRCh38
NC_000016.9:g.52586270T>C , CM000678.1:g.52586270T>C	GRCh37
NC_000016.8:g.51143771T>C	NCBI36
NG_012623.1:g.445A>G

Transcript Alleles

HGVS	Amino-acid Change
NR_033920.1:n.730A>G