Canonical Allele Identifier: CA452978339

Gene: ARID1B

Linked Data

• gnomAD v4: 6-157201322-G-T
• MyVariant Identifiers: chr6:g.157522456G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201322G>T , CM000668.2:g.157201322G>T	GRCh38
NC_000006.11:g.157522456G>T , CM000668.1:g.157522456G>T	GRCh37
NC_000006.10:g.157564148G>T	NCBI36
NG_032093.1:g.428393G>T
NG_032093.2:g.428393G>T
NG_066624.1:g.430297G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4938G>T	ENSP00000055163.8:p.Pro1646=
ENST00000414678.8:c.5007G>T	ENSP00000412835.3:p.Pro1669=
ENST00000637015.2:c.5226G>T	ENSP00000489729.2:p.Pro1742=
ENST00000346085.10:c.4977G>T	ENSP00000344546.5:p.Pro1659=
ENST00000350026.10:c.4689G>T	ENSP00000055163.7:p.Pro1563=
ENST00000414678.7:c.3255G>T	ENSP00000412835.2:p.Pro1085=
ENST00000635849.1:c.2418G>T	ENSP00000490948.1:p.Pro806=
ENST00000635957.1:c.2049G>T	ENSP00000490385.1:p.Pro683=
ENST00000636227.1:n.3560G>T
ENST00000636254.1:n.1017G>T
ENST00000636930.2:c.5097G>T MANE Select	ENSP00000490491.2:p.Pro1699=
ENST00000636940.1:n.3094G>T
ENST00000637015.1:c.2465G>T
ENST00000637568.1:c.2379G>T
ENST00000637741.1:n.1763G>T
ENST00000637810.1:c.2439G>T	ENSP00000489636.1:p.Pro813=
ENST00000637904.1:c.2598G>T	ENSP00000490550.1:p.Pro866=
ENST00000647938.1:c.4728G>T	ENSP00000498155.1:p.Pro1576=
ENST00000346085.9:c.4728G>T	ENSP00000344546.4:p.Pro1576=
ENST00000350026.9:c.4689G>T	ENSP00000055163.7:p.Pro1563=
ENST00000414678.6:c.3255G>T	ENSP00000412835.2:p.Pro1085=
NM_017519.2:c.4689G>T	NP_059989.2:p.Pro1563=
NM_020732.3:c.4728G>T	NP_065783.3:p.Pro1576=
XM_005267069.3:c.4848G>T	XP_005267126.2:p.Pro1616=
XM_011535984.1:c.3927G>T	XP_011534286.1:p.Pro1309=
XM_011535985.1:c.3747G>T	XP_011534287.1:p.Pro1249=
XM_011535986.1:c.3507G>T	XP_011534288.1:p.Pro1169=
XM_011535987.1:c.3126G>T	XP_011534289.1:p.Pro1042=
XM_011535988.1:c.1989G>T	XP_011534290.1:p.Pro663=
NM_001346813.1:c.4848G>T	NP_001333742.1:p.Pro1616=
NM_001363725.1:c.2598G>T	NP_001350654.1:p.Pro866=
XM_011535984.2:c.5058G>T	XP_011534286.2:p.Pro1686=
XM_011535988.3:c.1989G>T	XP_011534290.1:p.Pro663=
XM_017011103.2:c.4959G>T	XP_016866592.1:p.Pro1653=
XM_017011104.1:c.4929G>T	XP_016866593.1:p.Pro1643=
XM_017011105.2:c.4899G>T	XP_016866594.1:p.Pro1633=
XM_017011106.2:c.4770G>T	XP_016866595.1:p.Pro1590=
XM_017011107.2:c.4749G>T	XP_016866596.1:p.Pro1583=
XR_002956289.1:n.5044G>T
NM_001363725.2:c.2598G>T	NP_001350654.1:p.Pro866=
NM_001371656.1:c.4977G>T	NP_001358585.1:p.Pro1659=
NM_001374820.1:c.4977G>T	NP_001361749.1:p.Pro1659=
NM_001374828.1:c.5097G>T MANE Select	NP_001361757.1:p.Pro1699=
NM_017519.3:c.4938G>T	NP_059989.3:p.Pro1646=