Canonical Allele Identifier: CA1818352171

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127401006G= , CM000670.2:g.127401006G= GRCh38
NC_000008.10:g.128413251G= , CM000670.1:g.128413251G= GRCh37
NC_000008.9:g.128482433G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000645438.1:c.-559-13882G= (POU5F1B) ENSP00000495779.1:n.-559-13882G=
NR_109834.1:n.608G= (CCAT2)
NR_117100.1:n.1176+19823C= (CASC8)