Canonical Allele Identifier: CA1119017283
Gene: CASC11 HGNC NCBI

Linked Data

dbSNP Id: rs182311694

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127707454C>T , CM000670.2:g.127707454C>T GRCh38
NC_000008.10:g.128719699C>T , CM000670.1:g.128719699C>T GRCh37
NC_000008.9:g.128788881C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_117102.1:n.366-4211G>A