Canonical Allele Identifier: CA185773150
Gene: CASC11 HGNC NCBI

Linked Data

dbSNP Id: rs1018352174

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127705903G>A , CM000670.2:g.127705903G>A GRCh38
NC_000008.10:g.128718148G>A , CM000670.1:g.128718148G>A GRCh37
NC_000008.9:g.128787330G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_117102.1:n.366-2660C>T