Canonical Allele Identifier: CA1818352399

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127401111T= , CM000670.2:g.127401111T= GRCh38
NC_000008.10:g.128413356T= , CM000670.1:g.128413356T= GRCh37
NC_000008.9:g.128482538T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000645438.1:c.-559-13777T= ENSP00000495779.1:p.=
NR_109834.1:n.713T= (CCAT2)
NR_117100.1:n.1176+19718A= (CASC8)