Canonical Allele Identifier: CA1119017374
Gene: CASC11 HGNC NCBI

Linked Data

dbSNP Id: rs1815488235

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127707649A>G , CM000670.2:g.127707649A>G GRCh38
NC_000008.10:g.128719894A>G , CM000670.1:g.128719894A>G GRCh37
NC_000008.9:g.128789076A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_117102.1:n.366-4406T>C