Canonical Allele Identifier: CA1818486432
Gene: CASC11 HGNC NCBI

Linked Data

dbSNP Id: rs1815488756

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127707676T>A , CM000670.2:g.127707676T>A GRCh38
NC_000008.10:g.128719921T>A , CM000670.1:g.128719921T>A GRCh37
NC_000008.9:g.128789103T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_117102.1:n.366-4433A>T