Canonical Allele Identifier: CA185736844

Linked Data

dbSNP Id: rs866044986

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127401016C>T , CM000670.2:g.127401016C>T GRCh38
NC_000008.10:g.128413261C>T , CM000670.1:g.128413261C>T GRCh37
NC_000008.9:g.128482443C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000645438.1:c.-559-13872C>T (POU5F1B) ENSP00000495779.1:n.-559-13872C>T
NR_109834.1:n.618C>T (CCAT2)
NR_117100.1:n.1176+19813G>A (CASC8)