Canonical Allele Identifier: CA585078089
Gene: CASC11 HGNC NCBI

Linked Data

dbSNP Id: rs1245879794

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127707474A>G , CM000670.2:g.127707474A>G GRCh38
NC_000008.10:g.128719719A>G , CM000670.1:g.128719719A>G GRCh37
NC_000008.9:g.128788901A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_117102.1:n.366-4231T>C