Canonical Allele Identifier: CA293056421

Gene: CASC17

Linked Data

• dbSNP Id: rs779191511
• gnomAD v3: 17-71112758-A-G
• gnomAD v4: 17-71112758-A-G
• MyVariant Identifiers: chr17:g.69108899A>G (hg19) ; chr17:g.71112758A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.71112758A>G , CM000679.2:g.71112758A>G	GRCh38
NC_000017.10:g.69108899A>G , CM000679.1:g.69108899A>G	GRCh37
NC_000017.9:g.66620494A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_104152.1:n.218-13140T>C