Canonical Allele Identifier: CA1818319447

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127328736T= , CM000670.2:g.127328736T= GRCh38
NC_000008.10:g.128340981T= , CM000670.1:g.128340981T= GRCh37
NC_000008.9:g.128410163T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000645438.1:c.-715+6510T= (POU5F1B) ENSP00000495779.1:n.-715+6510T=
NR_117099.1:n.302+6510T= (CASC21)
NR_117100.1:n.1177-38676A= (CASC8)