Canonical Allele Identifier: CA622541154
Gene: CASC16 HGNC NCBI

Linked Data

dbSNP Id: rs1417463300
gnomAD v2: 16-52586389-T-G
gnomAD v3: 16-52552477-T-G
gnomAD v4: 16-52552477-T-G
MyVariant Identifiers: chr16:g.52586389T>G (hg19) chr16:g.52552477T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.52552477T>G , CM000678.2:g.52552477T>G GRCh38
NC_000016.9:g.52586389T>G , CM000678.1:g.52586389T>G GRCh37
NC_000016.8:g.51143890T>G NCBI36
NG_012623.1:g.326A>C

Transcript Alleles

HGVS Amino-acid change
NR_033920.1:n.654-43A>C
Search 100 bp 5'
Search 100 bp 3'