Canonical Allele Identifier: CA1818352120

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127400949A= , CM000670.2:g.127400949A= GRCh38
NC_000008.10:g.128413194A= , CM000670.1:g.128413194A= GRCh37
NC_000008.9:g.128482376A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000645438.1:c.-559-13939A= (POU5F1B) ENSP00000495779.1:n.-559-13939A=
NR_109834.1:n.551A= (CCAT2)
NR_117100.1:n.1176+19880T= (CASC8)