Canonical Allele Identifier: CA1914728785
Gene: EGR2 HGNC NCBI

Linked Data

dbSNP Id: rs224309

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.62848544A>G , CM000672.2:g.62848544A>G GRCh38
NC_000010.10:g.64608304A>G , CM000672.1:g.64608304A>G GRCh37
NC_000010.9:g.64278310A>G NCBI36
NG_008936.2:g.76357T>C , LRG_239:g.76357T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000493899.2:n.542-32575T>C
XM_011539428.1:c.-90-32575T>C XP_011537730.1:n.-90-32575T>C