Canonical Allele Identifier: CA1818319422

Linked Data

dbSNP Id: rs1813951458

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127328705C>T , CM000670.2:g.127328705C>T GRCh38
NC_000008.10:g.128340950C>T , CM000670.1:g.128340950C>T GRCh37
NC_000008.9:g.128410132C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000645438.1:c.-715+6479C>T (POU5F1B) ENSP00000495779.1:n.-715+6479C>T
NR_117099.1:n.302+6479C>T (CASC21)
NR_117100.1:n.1177-38645G>A (CASC8)