Canonical Allele Identifier: CA1818352610

Linked Data

dbSNP Id: rs1814935921

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127401302A>T , CM000670.2:g.127401302A>T GRCh38
NC_000008.10:g.128413547A>T , CM000670.1:g.128413547A>T GRCh37
NC_000008.9:g.128482729A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000645438.1:c.-559-13586A>T (POU5F1B) ENSP00000495779.1:n.-559-13586A>T
NR_109834.1:n.904A>T (CCAT2)
NR_117100.1:n.1176+19527T>A (CASC8)