Canonical Allele Identifier: CA774666241
Gene: CASC17 HGNC NCBI

Linked Data

dbSNP Id: rs1193296386
gnomAD v3: 17-71112420-T-G
gnomAD v4: 17-71112420-T-G
MyVariant Identifiers: chr17:g.69108561T>G (hg19) chr17:g.71112420T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.71112420T>G , CM000679.2:g.71112420T>G GRCh38
NC_000017.10:g.69108561T>G , CM000679.1:g.69108561T>G GRCh37
NC_000017.9:g.66620156T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_104152.1:n.218-12802A>C
Search 100 bp 5'
Search 100 bp 3'