Canonical Allele Identifier: CA479694087

Gene: ARID2

Linked Data

• gnomAD v4: 12-45852677-A-G
• MyVariant Identifiers: chr12:g.46246460A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.45852677A>G , CM000674.2:g.45852677A>G	GRCh38
NC_000012.11:g.46246460A>G , CM000674.1:g.46246460A>G	GRCh37
NC_000012.10:g.44532727A>G	NCBI36
NG_052800.1:g.128013A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422737.7:c.4554A>G	ENSP00000415650.3:p.Pro1518=
ENST00000457135.2:c.763A>G
ENST00000334344.11:c.4554A>G MANE Select	ENSP00000335044.6:p.Pro1518=
ENST00000422737.6:c.4475A>G
ENST00000334344.10:c.4554A>G	ENSP00000335044.6:p.Pro1518=
ENST00000422737.5:c.4107A>G	ENSP00000415650.1:p.Pro1369=
ENST00000444670.5:c.3384A>G	ENSP00000397307.1:p.Pro1128=
ENST00000457135.1:c.378A>G	ENSP00000388357.1:p.Pro126=
ENST00000479608.5:n.3845A>G
NM_152641.2:c.4554A>G	NP_689854.2:p.Pro1518=
XM_006719272.2:c.4554A>G	XP_006719335.1:p.Pro1518=
XM_011538025.1:c.2922A>G	XP_011536327.1:p.Pro974=
XR_944505.1:n.4702A>G
NM_001347839.1:c.4554A>G	NP_001334768.1:p.Pro1518=
NM_152641.3:c.4554A>G	NP_689854.2:p.Pro1518=
XM_006719272.4:c.4554A>G	XP_006719335.1:p.Pro1518=
XR_944505.3:n.4685A>G
NM_152641.4:c.4554A>G MANE Select	NP_689854.2:p.Pro1518=
NM_001347839.2:c.4554A>G	NP_001334768.1:p.Pro1518=