Canonical Allele Identifier: CA1818483898
Gene: CASC11 HGNC NCBI

Linked Data

dbSNP Id: rs1815453121

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127705661C>A , CM000670.2:g.127705661C>A GRCh38
NC_000008.10:g.128717906C>A , CM000670.1:g.128717906C>A GRCh37
NC_000008.9:g.128787088C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_117102.1:n.366-2418G>T