Canonical Allele Identifier: CA585068476

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127401035G>A , CM000670.2:g.127401035G>A GRCh38
NC_000008.10:g.128413280G>A , CM000670.1:g.128413280G>A GRCh37
NC_000008.9:g.128482462G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000645438.1:c.-559-13853G>A ENSP00000495779.1:p.=
NR_109834.1:n.637G>A (CCAT2)
NR_117100.1:n.1176+19794C>T (CASC8)