Canonical Allele Identifier: CA2579837139

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127400884A>C , CM000670.2:g.127400884A>C GRCh38
NC_000008.10:g.128413129A>C , CM000670.1:g.128413129A>C GRCh37
NC_000008.9:g.128482311A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000645438.1:c.-559-14004A>C (POU5F1B) ENSP00000495779.1:n.-559-14004A>C
NR_109834.1:n.486A>C (CCAT2)
NR_117100.1:n.1176+19945T>G (CASC8)