Canonical Allele Identifier: CA1818486399
Gene: CASC11 HGNC NCBI

Linked Data

dbSNP Id: rs1815488456

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127707665G>A , CM000670.2:g.127707665G>A GRCh38
NC_000008.10:g.128719910G>A , CM000670.1:g.128719910G>A GRCh37
NC_000008.9:g.128789092G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_117102.1:n.366-4422C>T