Canonical Allele Identifier: CA1818352180

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127401008G>A , CM000670.2:g.127401008G>A GRCh38
NC_000008.10:g.128413253G>A , CM000670.1:g.128413253G>A GRCh37
NC_000008.9:g.128482435G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000645438.1:c.-559-13880G>A ENSP00000495779.1:p.=
NR_109834.1:n.610G>A (CCAT2)
NR_117100.1:n.1176+19821C>T (CASC8)