Canonical Allele Identifier: CA185730420

Linked Data

dbSNP Id: rs1003686873

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127343329del , CM000670.2:g.127343329del GRCh38
NC_000008.10:g.128355575del , CM000670.1:g.128355575del GRCh37
NC_000008.9:g.128424757del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000645438.1:c.-560+3894del (POU5F1B) ENSP00000495779.1:n.-560+3894del
NR_117099.1:n.457+3894del (CASC21)
NR_117100.1:n.1177-53267del (CASC8)