Canonical Allele Identifier: CA1118993931

Linked Data

dbSNP Id: rs1814931504

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127400964C>T , CM000670.2:g.127400964C>T GRCh38
NC_000008.10:g.128413209C>T , CM000670.1:g.128413209C>T GRCh37
NC_000008.9:g.128482391C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000645438.1:c.-559-13924C>T (POU5F1B) ENSP00000495779.1:n.-559-13924C>T
NR_109834.1:n.566C>T (CCAT2)
NR_117100.1:n.1176+19865G>A (CASC8)