Canonical Allele Identifier: CA185736856

Linked Data

dbSNP Id: rs548390369

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127401111T>C , CM000670.2:g.127401111T>C GRCh38
NC_000008.10:g.128413356T>C , CM000670.1:g.128413356T>C GRCh37
NC_000008.9:g.128482538T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000645438.1:c.-559-13777T>C (POU5F1B) ENSP00000495779.1:n.-559-13777T>C
NR_109834.1:n.713T>C (CCAT2)
NR_117100.1:n.1176+19718A>G (CASC8)