Canonical Allele Identifier: CA2685463933

Gene: EZH2

Linked Data

• gnomAD v4: 7-148807374-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.148807374T>G , CM000669.2:g.148807374T>G	GRCh38
NC_000007.13:g.148504466T>G , CM000669.1:g.148504466T>G	GRCh37
NC_000007.12:g.148135399T>G	NCBI36
NG_032043.1:g.81976A>C , LRG_531:g.81976A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683292.1:c.*1424A>C	ENSP00000507503.1:n.*1424A>C
NM_001203247.1:c.*272A>C	NP_001190176.1:n.*272A>C
NM_001203248.1:c.*272A>C	NP_001190177.1:n.*272A>C
NM_001203249.1:c.*272A>C	NP_001190178.1:n.*272A>C
NM_004456.4:c.*272A>C , LRG_531t1:c.*272A>C	NP_004447.2:n.*272A>C
NM_152998.2:c.*272A>C	NP_694543.1:n.*272A>C
XM_005249962.3:c.*272A>C	XP_005250019.1:n.*272A>C
XM_005249963.3:c.*272A>C	XP_005250020.1:n.*272A>C
XM_005249964.3:c.*272A>C	XP_005250021.1:n.*272A>C
XM_011515883.1:c.*272A>C	XP_011514185.1:n.*272A>C
XM_011515884.1:c.*272A>C	XP_011514186.1:n.*272A>C
XM_011515885.1:c.*272A>C	XP_011514187.1:n.*272A>C
XM_011515886.1:c.*272A>C	XP_011514188.1:n.*272A>C
XM_011515887.1:c.*272A>C	XP_011514189.1:n.*272A>C
XM_011515888.1:c.*272A>C	XP_011514190.1:n.*272A>C
XM_011515889.1:c.*272A>C	XP_011514191.1:n.*272A>C
XM_011515890.1:c.*272A>C	XP_011514192.1:n.*272A>C
XM_011515891.1:c.*272A>C	XP_011514193.1:n.*272A>C
XM_011515892.1:c.*272A>C	XP_011514194.1:n.*272A>C
XM_011515893.1:c.*272A>C	XP_011514195.1:n.*272A>C
XM_011515894.1:c.*272A>C	XP_011514196.1:n.*272A>C
XM_011515895.1:c.*272A>C	XP_011514197.1:n.*272A>C
XM_011515896.1:c.*272A>C	XP_011514198.1:n.*272A>C
XM_011515897.1:c.*272A>C	XP_011514199.1:n.*272A>C
XM_011515898.1:c.*272A>C	XP_011514200.1:n.*272A>C
XR_928101.1:n.515+2289T>G
XR_928102.1:n.722+2289T>G
XR_002956413.1:n.5558A>C
XR_002956414.1:n.6018A>C