Canonical Allele Identifier: CA1818483990
Gene: CASC11 HGNC NCBI

Linked Data

dbSNP Id: rs1815453719

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127705700G>A , CM000670.2:g.127705700G>A GRCh38
NC_000008.10:g.128717945G>A , CM000670.1:g.128717945G>A GRCh37
NC_000008.9:g.128787127G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_117102.1:n.366-2457C>T