Canonical Allele Identifier: CA985992336
Gene: CASC17 HGNC NCBI

Linked Data

dbSNP Id: rs1908461379

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.71129372A>G , CM000679.2:g.71129372A>G GRCh38
NC_000017.10:g.69125513A>G , CM000679.1:g.69125513A>G GRCh37
NC_000017.9:g.66637108A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_104152.1:n.217+3018T>C