Canonical Allele Identifier: CA185736854

Linked Data

dbSNP Id: rs528595667

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127401091G>T , CM000670.2:g.127401091G>T GRCh38
NC_000008.10:g.128413336G>T , CM000670.1:g.128413336G>T GRCh37
NC_000008.9:g.128482518G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000645438.1:c.-559-13797G>T ENSP00000495779.1:p.=
NR_109834.1:n.693G>T (CCAT2)
NR_117100.1:n.1176+19738C>A (CASC8)