Canonical Allele Identifier: CA2579837164

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127400885T= , CM000670.2:g.127400885T= GRCh38
NC_000008.10:g.128413130T= , CM000670.1:g.128413130T= GRCh37
NC_000008.9:g.128482312T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000645438.1:c.-559-14003T= (POU5F1B) ENSP00000495779.1:n.-559-14003T=
NR_109834.1:n.487T= (CCAT2)
NR_117100.1:n.1176+19944A= (CASC8)