Canonical Allele Identifier: CA293056378

Gene: CASC17

Linked Data

• dbSNP Id: rs749404328
• gnomAD v3: 17-71112699-G-A
• gnomAD v4: 17-71112699-G-A
• MyVariant Identifiers: chr17:g.69108840G>A (hg19) ; chr17:g.71112699G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.71112699G>A , CM000679.2:g.71112699G>A	GRCh38
NC_000017.10:g.69108840G>A , CM000679.1:g.69108840G>A	GRCh37
NC_000017.9:g.66620435G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_104152.1:n.218-13081C>T