Canonical Allele Identifier: CA1119017371
Gene: CASC11 HGNC NCBI

Linked Data

dbSNP Id: rs1815487989

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127707631A>T , CM000670.2:g.127707631A>T GRCh38
NC_000008.10:g.128719876A>T , CM000670.1:g.128719876A>T GRCh37
NC_000008.9:g.128789058A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_117102.1:n.366-4388T>A