Canonical Allele Identifier: CA185736852

Linked Data

dbSNP Id: rs926272752

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127401082T>G , CM000670.2:g.127401082T>G GRCh38
NC_000008.10:g.128413327T>G , CM000670.1:g.128413327T>G GRCh37
NC_000008.9:g.128482509T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000645438.1:c.-559-13806T>G (POU5F1B) ENSP00000495779.1:n.-559-13806T>G
NR_109834.1:n.684T>G (CCAT2)
NR_117100.1:n.1176+19747A>C (CASC8)