Canonical Allele Identifier: CA1119017400
Gene: CASC11 HGNC NCBI

Linked Data

dbSNP Id: rs1815489872

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127707746_127707759del , CM000670.2:g.127707746_127707759del GRCh38
NC_000008.10:g.128719991_128720004del , CM000670.1:g.128719991_128720004del GRCh37
NC_000008.9:g.128789173_128789186del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_117102.1:n.366-4514_366-4501del