Canonical Allele Identifier: CA1818484223
Gene: CASC11 HGNC NCBI

Linked Data

dbSNP Id: rs1202318578

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127705866A>T , CM000670.2:g.127705866A>T GRCh38
NC_000008.10:g.128718111A>T , CM000670.1:g.128718111A>T GRCh37
NC_000008.9:g.128787293A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_117102.1:n.366-2623T>A