Canonical Allele Identifier: CA1818483890
Gene: CASC11 HGNC NCBI

Linked Data

dbSNP Id: rs1586576556

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127705649A>C , CM000670.2:g.127705649A>C GRCh38
NC_000008.10:g.128717894A>C , CM000670.1:g.128717894A>C GRCh37
NC_000008.9:g.128787076A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_117102.1:n.366-2406T>G