Canonical Allele Identifier: CA847153650

Linked Data

dbSNP Id: rs1411696722

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127401008G>T , CM000670.2:g.127401008G>T GRCh38
NC_000008.10:g.128413253G>T , CM000670.1:g.128413253G>T GRCh37
NC_000008.9:g.128482435G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000645438.1:c.-559-13880G>T (POU5F1B) ENSP00000495779.1:n.-559-13880G>T
NR_109834.1:n.610G>T (CCAT2)
NR_117100.1:n.1176+19821C>A (CASC8)