Canonical Allele Identifier: CA2579836985

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127401350A>G , CM000670.2:g.127401350A>G GRCh38
NC_000008.10:g.128413595A>G , CM000670.1:g.128413595A>G GRCh37
NC_000008.9:g.128482777A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000645438.1:c.-559-13538A>G (POU5F1B) ENSP00000495779.1:n.-559-13538A>G
NR_109834.1:n.952A>G (CCAT2)
NR_117100.1:n.1176+19479T>C (CASC8)