Canonical Allele Identifier: CA2718092342
Gene: CASC11 HGNC NCBI

Linked Data

dbSNP Id: rs57306986

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127705779G>T , CM000670.2:g.127705779G>T GRCh38
NC_000008.10:g.128718024G>T , CM000670.1:g.128718024G>T GRCh37
NC_000008.9:g.128787206G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_117102.1:n.366-2536C>A