Canonical Allele Identifier: CA1818352422

Genomic Alleles

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

Transcript Alleles

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