Canonical Allele Identifier: CA585068484

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127401085T>G , CM000670.2:g.127401085T>G GRCh38
NC_000008.10:g.128413330T>G , CM000670.1:g.128413330T>G GRCh37
NC_000008.9:g.128482512T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000645438.1:c.-559-13803T>G ENSP00000495779.1:p.=
NR_109834.1:n.687T>G (CCAT2)
NR_117100.1:n.1176+19744A>C (CASC8)