Canonical Allele Identifier: CA1818352835

Linked Data

dbSNP Id: rs1814938669

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127401525del , CM000670.2:g.127401525del GRCh38
NC_000008.10:g.128413770del , CM000670.1:g.128413770del GRCh37
NC_000008.9:g.128482952del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000645438.1:c.-559-13363del (POU5F1B) ENSP00000495779.1:n.-559-13363del
NR_109834.1:n.1127del (CCAT2)
NR_117100.1:n.1176+19304del (CASC8)