Canonical Allele Identifier: CA622658861
Gene: CASC16 HGNC NCBI

Linked Data

dbSNP Id: rs1242355059
gnomAD v2: 16-52586146-T-TC
gnomAD v3: 16-52552234-T-TC
gnomAD v4: 16-52552234-T-TC
MyVariant Identifiers: chr16:g.52586146_52586147insC (hg19) chr16:g.52552234_52552235insC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.52552238dup , CM000678.2:g.52552238dup GRCh38
NC_000016.9:g.52586150dup , CM000678.1:g.52586150dup GRCh37
NC_000016.8:g.51143651dup NCBI36
NG_012623.1:g.568dup

Transcript Alleles

HGVS Amino-acid change
NR_033920.1:n.853dup
Search 100 bp 5'
Search 100 bp 3'