Canonical Allele Identifier: CA585060486

Linked Data

dbSNP Id: rs1476426864

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127328836G>T , CM000670.2:g.127328836G>T GRCh38
NC_000008.10:g.128341081G>T , CM000670.1:g.128341081G>T GRCh37
NC_000008.9:g.128410263G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000645438.1:c.-715+6610G>T (POU5F1B) ENSP00000495779.1:n.-715+6610G>T
NR_117099.1:n.302+6610G>T (CASC21)
NR_117100.1:n.1177-38776C>A (CASC8)