Canonical Allele Identifier: CA185773140
Gene: CASC11 HGNC NCBI

Linked Data

dbSNP Id: rs9642880

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127705823G>T , CM000670.2:g.127705823G>T GRCh38
NC_000008.10:g.128718068G>T , CM000670.1:g.128718068G>T GRCh37
NC_000008.9:g.128787250G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_117102.1:n.366-2580C>A