Canonical Allele Identifier: CA294443497
Gene: CASC17 HGNC NCBI

Linked Data

dbSNP Id: rs576765547

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.71129470A>T , CM000679.2:g.71129470A>T GRCh38
NC_000017.10:g.69125611A>T , CM000679.1:g.69125611A>T GRCh37
NC_000017.9:g.66637206A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_104152.1:n.217+2920T>A