Canonical Allele Identifier: CA774666434

Gene: CASC17

Linked Data

• dbSNP Id: rs1487087938
• gnomAD v3: 17-71112746-G-C
• gnomAD v4: 17-71112746-G-C
• MyVariant Identifiers: chr17:g.69108887G>C (hg19) ; chr17:g.71112746G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.71112746G>C , CM000679.2:g.71112746G>C	GRCh38
NC_000017.10:g.69108887G>C , CM000679.1:g.69108887G>C	GRCh37
NC_000017.9:g.66620482G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_104152.1:n.218-13128C>G