Canonical Allele Identifier: CA585063558

Linked Data

dbSNP Id: rs1366130094

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127343300T>A , CM000670.2:g.127343300T>A GRCh38
NC_000008.10:g.128355546T>A , CM000670.1:g.128355546T>A GRCh37
NC_000008.9:g.128424728T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000645438.1:c.-560+3865T>A (POU5F1B) ENSP00000495779.1:n.-560+3865T>A
NR_117099.1:n.457+3865T>A (CASC21)
NR_117100.1:n.1177-53240A>T (CASC8)