Canonical Allele Identifier: CA847190333
Gene: CASC11 HGNC NCBI

Linked Data

dbSNP Id: rs1324741389

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127705798G>C , CM000670.2:g.127705798G>C GRCh38
NC_000008.10:g.128718043G>C , CM000670.1:g.128718043G>C GRCh37
NC_000008.9:g.128787225G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_117102.1:n.366-2555C>G