Canonical Allele Identifier: CA2222745330
Gene: CASC16 HGNC NCBI

Linked Data

dbSNP Id: rs1963297625

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.52552490T>C , CM000678.2:g.52552490T>C GRCh38
NC_000016.9:g.52586402T>C , CM000678.1:g.52586402T>C GRCh37
NC_000016.8:g.51143903T>C NCBI36
NG_012623.1:g.313A>G

Transcript Alleles

HGVS Amino-acid Change
NR_033920.1:n.654-56A>G