Canonical Allele Identifier: CA2579837589

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127401009G>C , CM000670.2:g.127401009G>C GRCh38
NC_000008.10:g.128413254G>C , CM000670.1:g.128413254G>C GRCh37
NC_000008.9:g.128482436G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000645438.1:c.-559-13879G>C (POU5F1B) ENSP00000495779.1:n.-559-13879G>C
NR_109834.1:n.611G>C (CCAT2)
NR_117100.1:n.1176+19820C>G (CASC8)