Canonical Allele Identifier: CA1818352441

Linked Data

dbSNP Id: rs1814933918

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127401135del , CM000670.2:g.127401135del GRCh38
NC_000008.10:g.128413380del , CM000670.1:g.128413380del GRCh37
NC_000008.9:g.128482562del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000645438.1:c.-559-13753del (POU5F1B) ENSP00000495779.1:n.-559-13753del
NR_109834.1:n.737del (CCAT2)
NR_117100.1:n.1176+19697del (CASC8)