Canonical Allele Identifier: CA2579836900

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127401321A= , CM000670.2:g.127401321A= GRCh38
NC_000008.10:g.128413566A= , CM000670.1:g.128413566A= GRCh37
NC_000008.9:g.128482748A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000645438.1:c.-559-13567A= (POU5F1B) ENSP00000495779.1:n.-559-13567A=
NR_109834.1:n.923A= (CCAT2)
NR_117100.1:n.1176+19508T= (CASC8)