Canonical Allele Identifier: CA185730391

Linked Data

dbSNP Id: rs771216976

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127343152A>T , CM000670.2:g.127343152A>T GRCh38
NC_000008.10:g.128355398A>T , CM000670.1:g.128355398A>T GRCh37
NC_000008.9:g.128424580A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000645438.1:c.-560+3717A>T (POU5F1B) ENSP00000495779.1:n.-560+3717A>T
NR_117099.1:n.457+3717A>T (CASC21)
NR_117100.1:n.1177-53092T>A (CASC8)