Canonical Allele Identifier: CA384492185

Gene: ARID2

Linked Data

• dbSNP Id: rs781147197
• gnomAD v2: 12-46246561-C-A
• gnomAD v4: 12-45852778-C-A
• MyVariant Identifiers: chr12:g.46246561C>A (hg19) ; chr12:g.45852778C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.45852778C>A , CM000674.2:g.45852778C>A	GRCh38
NC_000012.11:g.46246561C>A , CM000674.1:g.46246561C>A	GRCh37
NC_000012.10:g.44532828C>A	NCBI36
NG_052800.1:g.128114C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422737.7:c.4655C>A	ENSP00000415650.3:p.Thr1552Lys
ENST00000457135.2:c.864C>A
ENST00000334344.11:c.4655C>A MANE Select	ENSP00000335044.6:p.Thr1552Lys
ENST00000422737.6:c.4576C>A
ENST00000334344.10:c.4655C>A	ENSP00000335044.6:p.Thr1552Lys
ENST00000422737.5:c.4208C>A	ENSP00000415650.1:p.Thr1403Lys
ENST00000444670.5:c.3485C>A	ENSP00000397307.1:p.Thr1162Lys
ENST00000457135.1:c.479C>A	ENSP00000388357.1:p.Thr160Lys
ENST00000479608.5:n.3946C>A
NM_152641.2:c.4655C>A	NP_689854.2:p.Thr1552Lys
XM_006719272.2:c.4655C>A	XP_006719335.1:p.Thr1552Lys
XM_011538025.1:c.3023C>A	XP_011536327.1:p.Thr1008Lys
XR_944505.1:n.4803C>A
NM_001347839.1:c.4655C>A	NP_001334768.1:p.Thr1552Lys
NM_152641.3:c.4655C>A	NP_689854.2:p.Thr1552Lys
XM_006719272.4:c.4655C>A	XP_006719335.1:p.Thr1552Lys
XR_944505.3:n.4786C>A
NM_152641.4:c.4655C>A MANE Select	NP_689854.2:p.Thr1552Lys
NM_001347839.2:c.4655C>A	NP_001334768.1:p.Thr1552Lys