Canonical Allele Identifier: CA1818352576

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127401271A= , CM000670.2:g.127401271A= GRCh38
NC_000008.10:g.128413516A= , CM000670.1:g.128413516A= GRCh37
NC_000008.9:g.128482698A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000645438.1:c.-559-13617A= (POU5F1B) ENSP00000495779.1:n.-559-13617A=
NR_109834.1:n.873A= (CCAT2)
NR_117100.1:n.1176+19558T= (CASC8)