Canonical Allele Identifier: CA627484929

Gene: CASC17

Linked Data

• dbSNP Id: rs1349013533
• gnomAD v2: 17-69125615-G-T
• gnomAD v3: 17-71129474-G-T
• gnomAD v4: 17-71129474-G-T
• MyVariant Identifiers: chr17:g.69125615G>T (hg19) ; chr17:g.71129474G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.71129474G>T , CM000679.2:g.71129474G>T	GRCh38
NC_000017.10:g.69125615G>T , CM000679.1:g.69125615G>T	GRCh37
NC_000017.9:g.66637210G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_104152.1:n.217+2916C>A