Canonical Allele Identifier: CA168905158
Gene: EZH2 HGNC NCBI

Linked Data

dbSNP Id: rs778542064
MyVariant Identifiers: chr7:g.148504364T>G (hg19) chr7:g.148807272T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.148807272T>G , CM000669.2:g.148807272T>G GRCh38
NC_000007.13:g.148504364T>G , CM000669.1:g.148504364T>G GRCh37
NC_000007.12:g.148135297T>G NCBI36
NG_032043.1:g.82078A>C , LRG_531:g.82078A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000683292.1:c.*1526A>C ENSP00000507503.1:n.*1526A>C
XR_928101.1:n.515+2187T>G
XR_928102.1:n.722+2187T>G
Search 100 bp 5'
Search 100 bp 3'