Canonical Allele Identifier: CA2579837759

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127401068A= , CM000670.2:g.127401068A= GRCh38
NC_000008.10:g.128413313A= , CM000670.1:g.128413313A= GRCh37
NC_000008.9:g.128482495A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000645438.1:c.-559-13820A= (POU5F1B) ENSP00000495779.1:n.-559-13820A=
NR_109834.1:n.670A= (CCAT2)
NR_117100.1:n.1176+19761T= (CASC8)