Canonical Allele Identifier: CA294443520
Gene: CASC17 HGNC NCBI

Linked Data

dbSNP Id: rs1011622535

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.71129472T>G , CM000679.2:g.71129472T>G GRCh38
NC_000017.10:g.69125613T>G , CM000679.1:g.69125613T>G GRCh37
NC_000017.9:g.66637208T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_104152.1:n.217+2918A>C