Canonical Allele Identifier: CA384491734

Gene: ARID2

Linked Data

• dbSNP Id: rs1269556352
• gnomAD v2: 12-46246353-A-G
• gnomAD v4: 12-45852570-A-G
• MyVariant Identifiers: chr12:g.46246353A>G (hg19) ; chr12:g.45852570A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.45852570A>G , CM000674.2:g.45852570A>G	GRCh38
NC_000012.11:g.46246353A>G , CM000674.1:g.46246353A>G	GRCh37
NC_000012.10:g.44532620A>G	NCBI36
NG_052800.1:g.127906A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422737.7:c.4447A>G	ENSP00000415650.3:p.Ile1483Val
ENST00000457135.2:c.656A>G
ENST00000334344.11:c.4447A>G MANE Select	ENSP00000335044.6:p.Ile1483Val
ENST00000422737.6:c.4368A>G
ENST00000334344.10:c.4447A>G	ENSP00000335044.6:p.Ile1483Val
ENST00000422737.5:c.4000A>G	ENSP00000415650.1:p.Ile1334Val
ENST00000444670.5:c.3277A>G	ENSP00000397307.1:p.Ile1093Val
ENST00000457135.1:c.271A>G	ENSP00000388357.1:p.Ile91Val
ENST00000479608.5:n.3738A>G
NM_152641.2:c.4447A>G	NP_689854.2:p.Ile1483Val
XM_006719272.2:c.4447A>G	XP_006719335.1:p.Ile1483Val
XM_011538025.1:c.2815A>G	XP_011536327.1:p.Ile939Val
XR_944505.1:n.4595A>G
NM_001347839.1:c.4447A>G	NP_001334768.1:p.Ile1483Val
NM_152641.3:c.4447A>G	NP_689854.2:p.Ile1483Val
XM_006719272.4:c.4447A>G	XP_006719335.1:p.Ile1483Val
XR_944505.3:n.4578A>G
NM_152641.4:c.4447A>G MANE Select	NP_689854.2:p.Ile1483Val
NM_001347839.2:c.4447A>G	NP_001334768.1:p.Ile1483Val