Canonical Allele Identifier: CA6526696

Gene: ARID2

Linked Data

• dbSNP Id: rs765365503
• ExAC: 12:46246540 A / G
• gnomAD v2: 12-46246540-A-G
• gnomAD v3: 12-45852757-A-G
• gnomAD v4: 12-45852757-A-G
• MyVariant Identifiers: chr12:g.46246540A>G (hg19) ; chr12:g.45852757A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.45852757A>G , CM000674.2:g.45852757A>G	GRCh38
NC_000012.11:g.46246540A>G , CM000674.1:g.46246540A>G	GRCh37
NC_000012.10:g.44532807A>G	NCBI36
NG_052800.1:g.128093A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422737.7:c.4634A>G	ENSP00000415650.3:p.Asn1545Ser
ENST00000457135.2:c.843A>G
ENST00000334344.11:c.4634A>G MANE Select	ENSP00000335044.6:p.Asn1545Ser
ENST00000422737.6:c.4555A>G
ENST00000334344.10:c.4634A>G	ENSP00000335044.6:p.Asn1545Ser
ENST00000422737.5:c.4187A>G	ENSP00000415650.1:p.Asn1396Ser
ENST00000444670.5:c.3464A>G	ENSP00000397307.1:p.Asn1155Ser
ENST00000457135.1:c.458A>G	ENSP00000388357.1:p.Asn153Ser
ENST00000479608.5:n.3925A>G
NM_152641.2:c.4634A>G	NP_689854.2:p.Asn1545Ser
XM_006719272.2:c.4634A>G	XP_006719335.1:p.Asn1545Ser
XM_011538025.1:c.3002A>G	XP_011536327.1:p.Asn1001Ser
XR_944505.1:n.4782A>G
NM_001347839.1:c.4634A>G	NP_001334768.1:p.Asn1545Ser
NM_152641.3:c.4634A>G	NP_689854.2:p.Asn1545Ser
XM_006719272.4:c.4634A>G	XP_006719335.1:p.Asn1545Ser
XR_944505.3:n.4765A>G
NM_152641.4:c.4634A>G MANE Select	NP_689854.2:p.Asn1545Ser
NM_001347839.2:c.4634A>G	NP_001334768.1:p.Asn1545Ser