Canonical Allele Identifier: CA847153674

Linked Data

dbSNP Id: rs1348374963

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127401072G>C , CM000670.2:g.127401072G>C GRCh38
NC_000008.10:g.128413317G>C , CM000670.1:g.128413317G>C GRCh37
NC_000008.9:g.128482499G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000645438.1:c.-559-13816G>C (POU5F1B) ENSP00000495779.1:n.-559-13816G>C
NR_109834.1:n.674G>C (CCAT2)
NR_117100.1:n.1176+19757C>G (CASC8)