Canonical Allele Identifier: CA294443019

Gene: CASC17

Linked Data

• dbSNP Id: rs1038008078
• gnomAD v2: 17-69125524-G-A
• gnomAD v3: 17-71129383-G-A
• gnomAD v4: 17-71129383-G-A
• MyVariant Identifiers: chr17:g.69125524G>A (hg19) ; chr17:g.71129383G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.71129383G>A , CM000679.2:g.71129383G>A	GRCh38
NC_000017.10:g.69125524G>A , CM000679.1:g.69125524G>A	GRCh37
NC_000017.9:g.66637119G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_104152.1:n.217+3007C>T