Canonical Allele Identifier: CA185730439

Linked Data

dbSNP Id: rs955246312

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127343458A>G , CM000670.2:g.127343458A>G GRCh38
NC_000008.10:g.128355704A>G , CM000670.1:g.128355704A>G GRCh37
NC_000008.9:g.128424886A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000645438.1:c.-560+4023A>G (POU5F1B) ENSP00000495779.1:n.-560+4023A>G
NR_117099.1:n.457+4023A>G (CASC21)
NR_117100.1:n.1177-53398T>C (CASC8)