Canonical Allele Identifier: CA774676853
Gene: CASC17 HGNC NCBI

Linked Data

dbSNP Id: rs1439900091
MyVariant Identifiers: chr17:g.69125510T>C (hg19) chr17:g.71129369T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.71129369T>C , CM000679.2:g.71129369T>C GRCh38
NC_000017.10:g.69125510T>C , CM000679.1:g.69125510T>C GRCh37
NC_000017.9:g.66637105T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_104152.1:n.217+3021A>G
Search 100 bp 5'
Search 100 bp 3'