Canonical Allele Identifier: CA185773152
Gene: CASC11 HGNC NCBI

Linked Data

dbSNP Id: rs772659112

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127705930A>G , CM000670.2:g.127705930A>G GRCh38
NC_000008.10:g.128718175A>G , CM000670.1:g.128718175A>G GRCh37
NC_000008.9:g.128787357A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_117102.1:n.366-2687T>C