Canonical Allele Identifier: CA847160700

Linked Data

dbSNP Id: rs1313066130

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127343175A>G , CM000670.2:g.127343175A>G GRCh38
NC_000008.10:g.128355421A>G , CM000670.1:g.128355421A>G GRCh37
NC_000008.9:g.128424603A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000645438.1:c.-560+3740A>G (POU5F1B) ENSP00000495779.1:n.-560+3740A>G
NR_117099.1:n.457+3740A>G (CASC21)
NR_117100.1:n.1177-53115T>C (CASC8)