Canonical Allele Identifier: CA1818352183

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127401010T= , CM000670.2:g.127401010T= GRCh38
NC_000008.10:g.128413255T= , CM000670.1:g.128413255T= GRCh37
NC_000008.9:g.128482437T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000645438.1:c.-559-13878T= (POU5F1B) ENSP00000495779.1:n.-559-13878T=
NR_109834.1:n.612T= (CCAT2)
NR_117100.1:n.1176+19819A= (CASC8)