Canonical Allele Identifier: CA185728733

Linked Data

dbSNP Id: rs557979979

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127328818G>A , CM000670.2:g.127328818G>A GRCh38
NC_000008.10:g.128341063G>A , CM000670.1:g.128341063G>A GRCh37
NC_000008.9:g.128410245G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000645438.1:c.-715+6592G>A (POU5F1B) ENSP00000495779.1:n.-715+6592G>A
NR_117099.1:n.302+6592G>A (CASC21)
NR_117100.1:n.1177-38758C>T (CASC8)