Canonical Allele Identifier: CA1818352355

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127401073T= , CM000670.2:g.127401073T= GRCh38
NC_000008.10:g.128413318T= , CM000670.1:g.128413318T= GRCh37
NC_000008.9:g.128482500T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000645438.1:c.-559-13815T= (POU5F1B) ENSP00000495779.1:n.-559-13815T=
NR_109834.1:n.675T= (CCAT2)
NR_117100.1:n.1176+19756A= (CASC8)