Canonical Allele Identifier: CA1818352367

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127401082T= , CM000670.2:g.127401082T= GRCh38
NC_000008.10:g.128413327T= , CM000670.1:g.128413327T= GRCh37
NC_000008.9:g.128482509T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000645438.1:c.-559-13806T= ENSP00000495779.1:p.=
NR_109834.1:n.684T= (CCAT2)
NR_117100.1:n.1176+19747A= (CASC8)