Canonical Allele Identifier: CA847160828

Linked Data

dbSNP Id: rs1375014789

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127343455_127343456del , CM000670.2:g.127343455_127343456del GRCh38
NC_000008.10:g.128355701_128355702del , CM000670.1:g.128355701_128355702del GRCh37
NC_000008.9:g.128424883_128424884del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000645438.1:c.-560+4020_-560+4021del (POU5F1B) ENSP00000495779.1:n.-560+4020_-560+4021del
NR_117099.1:n.457+4020_457+4021del (CASC21)
NR_117100.1:n.1177-53394_1177-53393del (CASC8)