Canonical Allele Identifier: CA1818484297
Gene: CASC11 HGNC NCBI

Linked Data

dbSNP Id: rs1815458012

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127705936T>A , CM000670.2:g.127705936T>A GRCh38
NC_000008.10:g.128718181T>A , CM000670.1:g.128718181T>A GRCh37
NC_000008.9:g.128787363T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_117102.1:n.366-2693A>T