Canonical Allele Identifier: CA495704258
Gene: CASC16 HGNC NCBI

Linked Data

dbSNP Id: rs1284085305
MyVariant Identifiers: chr16:g.52586261G>A (hg19) chr16:g.52552349G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.52552349G>A , CM000678.2:g.52552349G>A GRCh38
NC_000016.9:g.52586261G>A , CM000678.1:g.52586261G>A GRCh37
NC_000016.8:g.51143762G>A NCBI36
NG_012623.1:g.454C>T

Transcript Alleles

HGVS Amino-acid change
NR_033920.1:n.739C>T
Search 100 bp 5'
Search 100 bp 3'