Canonical Allele Identifier: CA585068481

Linked Data

dbSNP Id: rs1382699280

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127401086del , CM000670.2:g.127401086del GRCh38
NC_000008.10:g.128413331del , CM000670.1:g.128413331del GRCh37
NC_000008.9:g.128482513del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000645438.1:c.-559-13802del (POU5F1B) ENSP00000495779.1:n.-559-13802del
NR_109834.1:n.688del (CCAT2)
NR_117100.1:n.1176+19747del (CASC8)