Canonical Allele Identifier: CA847153781

Linked Data

dbSNP Id: rs1465866144

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127401176del , CM000670.2:g.127401176del GRCh38
NC_000008.10:g.128413421del , CM000670.1:g.128413421del GRCh37
NC_000008.9:g.128482603del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000645438.1:c.-559-13712del (POU5F1B) ENSP00000495779.1:n.-559-13712del
NR_109834.1:n.778del (CCAT2)
NR_117100.1:n.1176+19655del (CASC8)