Canonical Allele Identifier: CA1818486213
Gene: CASC11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127707468T= , CM000670.2:g.127707468T= GRCh38
NC_000008.10:g.128719713T= , CM000670.1:g.128719713T= GRCh37
NC_000008.9:g.128788895T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_117102.1:n.366-4225A=