Canonical Allele Identifier: CA2579837200

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127401421T= , CM000670.2:g.127401421T= GRCh38
NC_000008.10:g.128413666T= , CM000670.1:g.128413666T= GRCh37
NC_000008.9:g.128482848T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000645438.1:c.-559-13467T= (POU5F1B) ENSP00000495779.1:n.-559-13467T=
NR_109834.1:n.1023T= (CCAT2)
NR_117100.1:n.1176+19408A= (CASC8)