Canonical Allele Identifier: CA1818352205

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127401027C= , CM000670.2:g.127401027C= GRCh38
NC_000008.10:g.128413272C= , CM000670.1:g.128413272C= GRCh37
NC_000008.9:g.128482454C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000645438.1:c.-559-13861C= (POU5F1B) ENSP00000495779.1:n.-559-13861C=
NR_109834.1:n.629C= (CCAT2)
NR_117100.1:n.1176+19802G= (CASC8)