Canonical Allele Identifier: CA185730438

Linked Data

dbSNP Id: rs192963991

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127343455A>G , CM000670.2:g.127343455A>G GRCh38
NC_000008.10:g.128355701A>G , CM000670.1:g.128355701A>G GRCh37
NC_000008.9:g.128424883A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000645438.1:c.-560+4020A>G (POU5F1B) ENSP00000495779.1:n.-560+4020A>G
NR_117099.1:n.457+4020A>G (CASC21)
NR_117100.1:n.1177-53395T>C (CASC8)