Canonical Allele Identifier: CA1119008325

Linked Data

dbSNP Id: rs1814141482

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127343331_127343333del , CM000670.2:g.127343331_127343333del GRCh38
NC_000008.10:g.128355577_128355579del , CM000670.1:g.128355577_128355579del GRCh37
NC_000008.9:g.128424759_128424761del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000645438.1:c.-560+3896_-560+3898del (POU5F1B) ENSP00000495779.1:n.-560+3896_-560+3898del
NR_117099.1:n.457+3896_457+3898del (CASC21)
NR_117100.1:n.1177-53273_1177-53271del (CASC8)