Canonical Allele Identifier: CA847153623

Linked Data

dbSNP Id: rs1319467484

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127400924del , CM000670.2:g.127400924del GRCh38
NC_000008.10:g.128413169del , CM000670.1:g.128413169del GRCh37
NC_000008.9:g.128482351del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000645438.1:c.-559-13964del (POU5F1B) ENSP00000495779.1:n.-559-13964del
NR_109834.1:n.526del (CCAT2)
NR_117100.1:n.1176+19905del (CASC8)