Canonical Allele Identifier: CA1751419015
Gene: EZH2 HGNC NCBI

Linked Data

dbSNP Id: rs1801716554

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.148807274A>C , CM000669.2:g.148807274A>C GRCh38
NC_000007.13:g.148504366A>C , CM000669.1:g.148504366A>C GRCh37
NC_000007.12:g.148135299A>C NCBI36
NG_032043.1:g.82076T>G , LRG_531:g.82076T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000683292.1:c.*1524T>G ENSP00000507503.1:n.*1524T>G
XR_928101.1:n.515+2189A>C
XR_928102.1:n.722+2189A>C