Canonical Allele Identifier: CA281875496
Gene: CASC16 HGNC NCBI

Linked Data

dbSNP Id: rs1016454100
MyVariant Identifiers: chr16:g.52552462A>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.52552462A>G , CM000678.2:g.52552462A>G GRCh38
NC_000016.9:g.52586374A>G , CM000678.1:g.52586374A>G GRCh37
NC_000016.8:g.51143875A>G NCBI36
NG_012623.1:g.341T>C

Transcript Alleles

HGVS Amino-acid change
NR_033920.1:n.654-28T>C