Canonical Allele Identifier: CA1119008281

Linked Data

dbSNP Id: rs1814141034

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127343316del , CM000670.2:g.127343316del GRCh38
NC_000008.10:g.128355562del , CM000670.1:g.128355562del GRCh37
NC_000008.9:g.128424744del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000645438.1:c.-560+3881del (POU5F1B) ENSP00000495779.1:n.-560+3881del
NR_117099.1:n.457+3881del (CASC21)
NR_117100.1:n.1177-53256del (CASC8)