Canonical Allele Identifier: CA293056222

Gene: CASC17

Linked Data

• dbSNP Id: rs946217824
• gnomAD v2: 17-69108532-G-A
• gnomAD v3: 17-71112391-G-A
• gnomAD v4: 17-71112391-G-A
• MyVariant Identifiers: chr17:g.69108532G>A (hg19) ; chr17:g.71112391G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.71112391G>A , CM000679.2:g.71112391G>A	GRCh38
NC_000017.10:g.69108532G>A , CM000679.1:g.69108532G>A	GRCh37
NC_000017.9:g.66620127G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_104152.1:n.218-12773C>T