Canonical Allele Identifier: CA2579837203

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127401421T>G , CM000670.2:g.127401421T>G GRCh38
NC_000008.10:g.128413666T>G , CM000670.1:g.128413666T>G GRCh37
NC_000008.9:g.128482848T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000645438.1:c.-559-13467T>G (POU5F1B) ENSP00000495779.1:n.-559-13467T>G
NR_109834.1:n.1023T>G (CCAT2)
NR_117100.1:n.1176+19408A>C (CASC8)