Canonical Allele Identifier: CA366234841

Gene: ARID1B

Linked Data

• ClinVar Variation Id: 2053259
• ClinVar RCV Id: RCV002938078
• MyVariant Identifiers: chr6:g.157511195A>G (hg19) ; chr6:g.157190061A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190061A>G , CM000668.2:g.157190061A>G	GRCh38
NC_000006.11:g.157511195A>G , CM000668.1:g.157511195A>G	GRCh37
NC_000006.10:g.157552887A>G	NCBI36
NG_032093.1:g.417132A>G
NG_032093.2:g.417132A>G
NG_066624.1:g.419036A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3923A>G	ENSP00000055163.8:p.Asp1308Gly
ENST00000414678.8:c.3992A>G	ENSP00000412835.3:p.Asp1331Gly
ENST00000637015.2:c.4211A>G	ENSP00000489729.2:p.Asp1404Gly
ENST00000346085.10:c.3962A>G	ENSP00000344546.5:p.Asp1321Gly
ENST00000350026.10:c.3674A>G	ENSP00000055163.7:p.Asp1225Gly
ENST00000414678.7:c.2240A>G	ENSP00000412835.2:p.Asp747Gly
ENST00000635849.1:c.1403A>G	ENSP00000490948.1:p.Asp468Gly
ENST00000635957.1:c.1034A>G	ENSP00000490385.1:p.Asp345Gly
ENST00000636930.2:c.4082A>G MANE Select	ENSP00000490491.2:p.Asp1361Gly
ENST00000636940.1:n.2079A>G
ENST00000637015.1:c.1450A>G
ENST00000637568.1:c.1364A>G
ENST00000637741.1:n.748A>G
ENST00000637810.1:c.1424A>G	ENSP00000489636.1:p.Asp475Gly
ENST00000637904.1:c.1583A>G	ENSP00000490550.1:p.Asp528Gly
ENST00000647938.1:c.3713A>G	ENSP00000498155.1:p.Asp1238Gly
ENST00000346085.9:c.3713A>G	ENSP00000344546.4:p.Asp1238Gly
ENST00000350026.9:c.3674A>G	ENSP00000055163.7:p.Asp1225Gly
ENST00000414678.6:c.2240A>G	ENSP00000412835.2:p.Asp747Gly
NM_017519.2:c.3674A>G	NP_059989.2:p.Asp1225Gly
NM_020732.3:c.3713A>G	NP_065783.3:p.Asp1238Gly
XM_005267069.3:c.3833A>G	XP_005267126.2:p.Asp1278Gly
XM_011535984.1:c.2912A>G	XP_011534286.1:p.Asp971Gly
XM_011535985.1:c.2732A>G	XP_011534287.1:p.Asp911Gly
XM_011535986.1:c.2492A>G	XP_011534288.1:p.Asp831Gly
XM_011535987.1:c.2111A>G	XP_011534289.1:p.Asp704Gly
XM_011535988.1:c.974A>G	XP_011534290.1:p.Asp325Gly
NM_001346813.1:c.3833A>G	NP_001333742.1:p.Asp1278Gly
NM_001363725.1:c.1583A>G	NP_001350654.1:p.Asp528Gly
XM_011535984.2:c.4043A>G	XP_011534286.2:p.Asp1348Gly
XM_011535988.3:c.974A>G	XP_011534290.1:p.Asp325Gly
XM_017011103.2:c.3944A>G	XP_016866592.1:p.Asp1315Gly
XM_017011104.1:c.3914A>G	XP_016866593.1:p.Asp1305Gly
XM_017011105.2:c.3884A>G	XP_016866594.1:p.Asp1295Gly
XM_017011106.2:c.3755A>G	XP_016866595.1:p.Asp1252Gly
XM_017011107.2:c.3734A>G	XP_016866596.1:p.Asp1245Gly
XR_002956289.1:n.4126A>G
NM_001363725.2:c.1583A>G	NP_001350654.1:p.Asp528Gly
NM_001371656.1:c.3962A>G	NP_001358585.1:p.Asp1321Gly
NM_001374820.1:c.3962A>G	NP_001361749.1:p.Asp1321Gly
NM_001374828.1:c.4082A>G MANE Select	NP_001361757.1:p.Asp1361Gly
NM_017519.3:c.3923A>G	NP_059989.3:p.Asp1308Gly