Canonical Allele Identifier: CA281875482
Gene: CASC16 HGNC NCBI

Linked Data

dbSNP Id: rs562849244
gnomAD v2: 16-52586276-C-G
gnomAD v3: 16-52552364-C-G
gnomAD v4: 16-52552364-C-G
MyVariant Identifiers: chr16:g.52586276C>G (hg19) chr16:g.52552364C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.52552364C>G , CM000678.2:g.52552364C>G GRCh38
NC_000016.9:g.52586276C>G , CM000678.1:g.52586276C>G GRCh37
NC_000016.8:g.51143777C>G NCBI36
NG_012623.1:g.439G>C

Transcript Alleles

HGVS Amino-acid Change
NR_033920.1:n.724G>C
Search 100 bp 5'
Search 100 bp 3'