Canonical Allele Identifier: CA6526666

Gene: ARID2

Linked Data

• dbSNP Id: rs770783586
• ExAC: 12:46246367 C / T
• gnomAD v2: 12-46246367-C-T
• gnomAD v3: 12-45852584-C-T
• gnomAD v4: 12-45852584-C-T
• MyVariant Identifiers: chr12:g.46246367C>T (hg19) ; chr12:g.45852584C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.45852584C>T , CM000674.2:g.45852584C>T	GRCh38
NC_000012.11:g.46246367C>T , CM000674.1:g.46246367C>T	GRCh37
NC_000012.10:g.44532634C>T	NCBI36
NG_052800.1:g.127920C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422737.7:c.4461C>T	ENSP00000415650.3:p.Pro1487=
ENST00000457135.2:c.670C>T
ENST00000334344.11:c.4461C>T MANE Select	ENSP00000335044.6:p.Pro1487=
ENST00000422737.6:c.4382C>T
ENST00000334344.10:c.4461C>T	ENSP00000335044.6:p.Pro1487=
ENST00000422737.5:c.4014C>T	ENSP00000415650.1:p.Pro1338=
ENST00000444670.5:c.3291C>T	ENSP00000397307.1:p.Pro1097=
ENST00000457135.1:c.285C>T	ENSP00000388357.1:p.Pro95=
ENST00000479608.5:n.3752C>T
NM_152641.2:c.4461C>T	NP_689854.2:p.Pro1487=
XM_006719272.2:c.4461C>T	XP_006719335.1:p.Pro1487=
XM_011538025.1:c.2829C>T	XP_011536327.1:p.Pro943=
XR_944505.1:n.4609C>T
NM_001347839.1:c.4461C>T	NP_001334768.1:p.Pro1487=
NM_152641.3:c.4461C>T	NP_689854.2:p.Pro1487=
XM_006719272.4:c.4461C>T	XP_006719335.1:p.Pro1487=
XR_944505.3:n.4592C>T
NM_152641.4:c.4461C>T MANE Select	NP_689854.2:p.Pro1487=
NM_001347839.2:c.4461C>T	NP_001334768.1:p.Pro1487=