Canonical Allele Identifier: CA185773153
Gene: CASC11 HGNC NCBI

Linked Data

dbSNP Id: rs141683996

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127705938G>A , CM000670.2:g.127705938G>A GRCh38
NC_000008.10:g.128718183G>A , CM000670.1:g.128718183G>A GRCh37
NC_000008.9:g.128787365G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_117102.1:n.366-2695C>T