Canonical Allele Identifier: CA2579837594

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127401011G>T , CM000670.2:g.127401011G>T GRCh38
NC_000008.10:g.128413256G>T , CM000670.1:g.128413256G>T GRCh37
NC_000008.9:g.128482438G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000645438.1:c.-559-13877G>T (POU5F1B) ENSP00000495779.1:n.-559-13877G>T
NR_109834.1:n.613G>T (CCAT2)
NR_117100.1:n.1176+19818C>A (CASC8)