Canonical Allele Identifier: CA1751419090
Gene: EZH2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.148807373A= , CM000669.2:g.148807373A= GRCh38
NC_000007.13:g.148504465A= , CM000669.1:g.148504465A= GRCh37
NC_000007.12:g.148135398A= NCBI36
NG_032043.1:g.81977T= , LRG_531:g.81977T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000683292.1:c.*1425T= ENSP00000507503.1:n.*1425T=
NM_001203247.1:c.*273T= NP_001190176.1:n.*273T=
NM_001203248.1:c.*273T= NP_001190177.1:n.*273T=
NM_001203249.1:c.*273T= NP_001190178.1:n.*273T=
NM_004456.4:c.*273T= , LRG_531t1:c.*273T= NP_004447.2:n.*273T=
NM_152998.2:c.*273T= NP_694543.1:n.*273T=
XR_928101.1:n.515+2288A=
XR_928102.1:n.722+2288A=
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