Canonical Allele Identifier: CA1118994067

Linked Data

dbSNP Id: rs1397322531

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127401102T>C , CM000670.2:g.127401102T>C GRCh38
NC_000008.10:g.128413347T>C , CM000670.1:g.128413347T>C GRCh37
NC_000008.9:g.128482529T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000645438.1:c.-559-13786T>C (POU5F1B) ENSP00000495779.1:n.-559-13786T>C
NR_109834.1:n.704T>C (CCAT2)
NR_117100.1:n.1176+19727A>G (CASC8)