Canonical Allele Identifier: CA15552728

Linked Data

dbSNP Id: rs2392780

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127375779A>G , CM000670.2:g.127375779A>G GRCh38
NC_000008.10:g.128388025A>G , CM000670.1:g.128388025A>G GRCh37
NC_000008.9:g.128457207A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000645438.1:c.-560+36344A>G (POU5F1B) ENSP00000495779.1:n.-560+36344A>G
NR_117099.1:n.458-16725A>G (CASC21)
NR_117100.1:n.1176+45050T>C (CASC8)