Canonical Allele Identifier: CA1119016807
Gene: CASC11 HGNC NCBI

Linked Data

dbSNP Id: rs1815456642

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127705856_127705857insA , CM000670.2:g.127705856_127705857insA GRCh38
NC_000008.10:g.128718101_128718102insA , CM000670.1:g.128718101_128718102insA GRCh37
NC_000008.9:g.128787283_128787284insA NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_117102.1:n.366-2614_366-2613insT