Canonical Allele Identifier: CA1818352215

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127401033T>A , CM000670.2:g.127401033T>A GRCh38
NC_000008.10:g.128413278T>A , CM000670.1:g.128413278T>A GRCh37
NC_000008.9:g.128482460T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000645438.1:c.-559-13855T>A ENSP00000495779.1:p.=
NR_109834.1:n.635T>A (CCAT2)
NR_117100.1:n.1176+19796A>T (CASC8)