Canonical Allele Identifier: CA1818352162

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127400991T>C , CM000670.2:g.127400991T>C GRCh38
NC_000008.10:g.128413236T>C , CM000670.1:g.128413236T>C GRCh37
NC_000008.9:g.128482418T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000645438.1:c.-559-13897T>C ENSP00000495779.1:p.=
NR_109834.1:n.593T>C (CCAT2)
NR_117100.1:n.1176+19838A>G (CASC8)