Canonical Allele Identifier: CA585077712
Gene: CASC11 HGNC NCBI

Linked Data

dbSNP Id: rs950005928

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127705853T>A , CM000670.2:g.127705853T>A GRCh38
NC_000008.10:g.128718098T>A , CM000670.1:g.128718098T>A GRCh37
NC_000008.9:g.128787280T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_117102.1:n.366-2610A>T