Canonical Allele Identifier: CA2273435999
Gene: CASC17 HGNC NCBI

Linked Data

dbSNP Id: rs1908472873

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.71129507G>T , CM000679.2:g.71129507G>T GRCh38
NC_000017.10:g.69125648G>T , CM000679.1:g.69125648G>T GRCh37
NC_000017.9:g.66637243G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_104152.1:n.217+2883C>A