Canonical Allele Identifier: CA1818352424

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127401121G>A , CM000670.2:g.127401121G>A GRCh38
NC_000008.10:g.128413366G>A , CM000670.1:g.128413366G>A GRCh37
NC_000008.9:g.128482548G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000645438.1:c.-559-13767G>A ENSP00000495779.1:p.=
NR_109834.1:n.723G>A (CCAT2)
NR_117100.1:n.1176+19708C>T (CASC8)