Canonical Allele Identifier: CA185730404

Linked Data

dbSNP Id: rs922505203

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127343261G>A , CM000670.2:g.127343261G>A GRCh38
NC_000008.10:g.128355507G>A , CM000670.1:g.128355507G>A GRCh37
NC_000008.9:g.128424689G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000645438.1:c.-560+3826G>A (POU5F1B) ENSP00000495779.1:n.-560+3826G>A
NR_117099.1:n.457+3826G>A (CASC21)
NR_117100.1:n.1177-53201C>T (CASC8)