Canonical Allele Identifier: CA1751419022
Gene: EZH2 HGNC NCBI

Linked Data

dbSNP Id: rs1725606487

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.148807284C>A , CM000669.2:g.148807284C>A GRCh38
NC_000007.13:g.148504376C>A , CM000669.1:g.148504376C>A GRCh37
NC_000007.12:g.148135309C>A NCBI36
NG_032043.1:g.82066G>T , LRG_531:g.82066G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000683292.1:c.*1514G>T ENSP00000507503.1:n.*1514G>T
XR_928101.1:n.515+2199C>A
XR_928102.1:n.722+2199C>A