Canonical Allele Identifier: CA495703648
Gene: CASC16 HGNC NCBI

Linked Data

dbSNP Id: rs1347901801
gnomAD v2: 16-52586153-G-T
gnomAD v3: 16-52552241-G-T
gnomAD v4: 16-52552241-G-T
MyVariant Identifiers: chr16:g.52586153G>T (hg19) chr16:g.52552241G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.52552241G>T , CM000678.2:g.52552241G>T GRCh38
NC_000016.9:g.52586153G>T , CM000678.1:g.52586153G>T GRCh37
NC_000016.8:g.51143654G>T NCBI36
NG_012623.1:g.562C>A

Transcript Alleles

HGVS Amino-acid change
NR_033920.1:n.847C>A
Search 100 bp 5'
Search 100 bp 3'