Canonical Allele Identifier: CA774676862
Gene: CASC17 HGNC NCBI

Linked Data

dbSNP Id: rs1360880243
MyVariant Identifiers: chr17:g.69125517T>A (hg19) chr17:g.71129376T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.71129376T>A , CM000679.2:g.71129376T>A GRCh38
NC_000017.10:g.69125517T>A , CM000679.1:g.69125517T>A GRCh37
NC_000017.9:g.66637112T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_104152.1:n.217+3014A>T
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