Canonical Allele Identifier: CA185773355
Gene: CASC11 HGNC NCBI

Linked Data

dbSNP Id: rs952578009

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127707658T>C , CM000670.2:g.127707658T>C GRCh38
NC_000008.10:g.128719903T>C , CM000670.1:g.128719903T>C GRCh37
NC_000008.9:g.128789085T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_117102.1:n.366-4415A>G