Canonical Allele Identifier: CA1818335357

Linked Data

dbSNP Id: rs1814138628

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127343137_127343138insTG , CM000670.2:g.127343137_127343138insTG GRCh38
NC_000008.10:g.128355383_128355384insTG , CM000670.1:g.128355383_128355384insTG GRCh37
NC_000008.9:g.128424565_128424566insTG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000645438.1:c.-560+3702_-560+3703insTG (POU5F1B) ENSP00000495779.1:n.-560+3702_-560+3703insTG
NR_117099.1:n.457+3702_457+3703insTG (CASC21)
NR_117100.1:n.1177-53078_1177-53077insCA (CASC8)