Canonical Allele Identifier: CA168905157
Gene: EZH2 HGNC NCBI

Linked Data

dbSNP Id: rs912178387

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.148807258C>T , CM000669.2:g.148807258C>T GRCh38
NC_000007.13:g.148504350C>T , CM000669.1:g.148504350C>T GRCh37
NC_000007.12:g.148135283C>T NCBI36
NG_032043.1:g.82092G>A , LRG_531:g.82092G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000683292.1:c.*1540G>A ENSP00000507503.1:n.*1540G>A
XR_928101.1:n.515+2173C>T
XR_928102.1:n.722+2173C>T