Canonical Allele Identifier: CA2688553292

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127401122del , CM000670.2:g.127401122del GRCh38
NC_000008.10:g.128413367del , CM000670.1:g.128413367del GRCh37
NC_000008.9:g.128482549del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000645438.1:c.-559-13766del (POU5F1B) ENSP00000495779.1:n.-559-13766del
NR_109834.1:n.724del (CCAT2)
NR_117100.1:n.1176+19707del (CASC8)