Canonical Allele Identifier: CA185736851

Linked Data

dbSNP Id: rs766119038

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127401081A>G , CM000670.2:g.127401081A>G GRCh38
NC_000008.10:g.128413326A>G , CM000670.1:g.128413326A>G GRCh37
NC_000008.9:g.128482508A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000645438.1:c.-559-13807A>G (POU5F1B) ENSP00000495779.1:n.-559-13807A>G
NR_109834.1:n.683A>G (CCAT2)
NR_117100.1:n.1176+19748T>C (CASC8)