Canonical Allele Identifier: CA185736840

Linked Data

dbSNP Id: rs1032627092

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127400961T>C , CM000670.2:g.127400961T>C GRCh38
NC_000008.10:g.128413206T>C , CM000670.1:g.128413206T>C GRCh37
NC_000008.9:g.128482388T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000645438.1:c.-559-13927T>C (POU5F1B) ENSP00000495779.1:n.-559-13927T>C
NR_109834.1:n.563T>C (CCAT2)
NR_117100.1:n.1176+19868A>G (CASC8)