Canonical Allele Identifier: CA2579836522

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127401197G>C , CM000670.2:g.127401197G>C GRCh38
NC_000008.10:g.128413442G>C , CM000670.1:g.128413442G>C GRCh37
NC_000008.9:g.128482624G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000645438.1:c.-559-13691G>C (POU5F1B) ENSP00000495779.1:n.-559-13691G>C
NR_109834.1:n.799G>C (CCAT2)
NR_117100.1:n.1176+19632C>G (CASC8)