Canonical Allele Identifier: CA847190321
Gene: CASC11 HGNC NCBI

Linked Data

dbSNP Id: rs1439823683

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127705783A>G , CM000670.2:g.127705783A>G GRCh38
NC_000008.10:g.128718028A>G , CM000670.1:g.128718028A>G GRCh37
NC_000008.9:g.128787210A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_117102.1:n.366-2540T>C