Canonical Allele Identifier: CA594034006

Gene: EGR2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.62896153G>T , CM000672.2:g.62896153G>T	GRCh38
NC_000010.10:g.64655913G>T , CM000672.1:g.64655913G>T	GRCh37
NC_000010.9:g.64325919G>T	NCBI36
NG_008936.2:g.28748C>A , LRG_239:g.28748C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000493899.2:n.417-1616C>A
XM_011539428.1:c.-215-1616C>A	XP_011537730.1:n.-215-1616C>A
XR_001747465.1:n.424-1616C>A
XR_001747466.1:n.424-601C>A