Canonical Allele Identifier: CA495703599
Gene: CASC16 HGNC NCBI

Linked Data

dbSNP Id: rs1350149066
MyVariant Identifiers: chr16:g.52586144T>C (hg19) chr16:g.52552232T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.52552232T>C , CM000678.2:g.52552232T>C GRCh38
NC_000016.9:g.52586144T>C , CM000678.1:g.52586144T>C GRCh37
NC_000016.8:g.51143645T>C NCBI36
NG_012623.1:g.571A>G

Transcript Alleles

HGVS Amino-acid Change
NR_033920.1:n.856A>G
Search 100 bp 5'
Search 100 bp 3'