Canonical Allele Identifier: CA977368908
Gene: CASC16 HGNC NCBI

Linked Data

dbSNP Id: rs1963449413
gnomAD v3: 16-52567292-A-C
gnomAD v4: 16-52567292-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.52567292A>C , CM000678.2:g.52567292A>C GRCh38
NC_000016.9:g.52601204A>C , CM000678.1:g.52601204A>C GRCh37
NC_000016.8:g.51158705A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_033920.1:n.605-4430T>G
Search 100 bp 5'
Search 100 bp 3'