Canonical Allele Identifier: CA847160745

Linked Data

dbSNP Id: rs1456563895

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127343305dup , CM000670.2:g.127343305dup GRCh38
NC_000008.10:g.128355551dup , CM000670.1:g.128355551dup GRCh37
NC_000008.9:g.128424733dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000645438.1:c.-560+3870dup (POU5F1B) ENSP00000495779.1:n.-560+3870dup
NR_117099.1:n.457+3870dup (CASC21)
NR_117100.1:n.1177-53245dup (CASC8)