Canonical Allele Identifier: CA185730421

Linked Data

dbSNP Id: rs901721810

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127343331C>T , CM000670.2:g.127343331C>T GRCh38
NC_000008.10:g.128355577C>T , CM000670.1:g.128355577C>T GRCh37
NC_000008.9:g.128424759C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000645438.1:c.-560+3896C>T (POU5F1B) ENSP00000495779.1:n.-560+3896C>T
NR_117099.1:n.457+3896C>T (CASC21)
NR_117100.1:n.1177-53271G>A (CASC8)