Canonical Allele Identifier: CA13156857
Gene: EGR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.62820815C>T , CM000672.2:g.62820815C>T GRCh38
NC_000010.10:g.64580575C>T , CM000672.1:g.64580575C>T GRCh37
NC_000010.9:g.64250581C>T NCBI36
NG_008936.2:g.104086G>A , LRG_239:g.104086G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000493899.2:n.542-4846G>A
XM_011539428.1:c.-90-4846G>A XP_011537730.1:n.-90-4846G>A