Canonical Allele Identifier: CA1818486291
Gene: CASC11 HGNC NCBI

Linked Data

dbSNP Id: rs1815487144

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127707547C>A , CM000670.2:g.127707547C>A GRCh38
NC_000008.10:g.128719792C>A , CM000670.1:g.128719792C>A GRCh37
NC_000008.9:g.128788974C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_117102.1:n.366-4304G>T