Canonical Allele Identifier: CA2718232892
Gene: CASC11 HGNC NCBI

Linked Data

dbSNP Id: rs2130030957

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127705963A>G , CM000670.2:g.127705963A>G GRCh38
NC_000008.10:g.128718208A>G , CM000670.1:g.128718208A>G GRCh37
NC_000008.9:g.128787390A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_117102.1:n.366-2720T>C