Canonical Allele Identifier: CA1119017387
Gene: CASC11 HGNC NCBI

Linked Data

dbSNP Id: rs890961978

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127707672T>C , CM000670.2:g.127707672T>C GRCh38
NC_000008.10:g.128719917T>C , CM000670.1:g.128719917T>C GRCh37
NC_000008.9:g.128789099T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_117102.1:n.366-4429A>G