Canonical Allele Identifier: CA4067710

Gene: ARID1B

Linked Data

• dbSNP Id: rs373500669
• ExAC: 6:157522152 A / G
• gnomAD v2: 6-157522152-A-G
• gnomAD v3: 6-157201018-A-G
• gnomAD v4: 6-157201018-A-G
• MyVariant Identifiers: chr6:g.157522152A>G (hg19) ; chr6:g.157201018A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201018A>G , CM000668.2:g.157201018A>G	GRCh38
NC_000006.11:g.157522152A>G , CM000668.1:g.157522152A>G	GRCh37
NC_000006.10:g.157563844A>G	NCBI36
NG_032093.1:g.428089A>G
NG_032093.2:g.428089A>G
NG_066624.1:g.429993A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4634A>G	ENSP00000055163.8:p.Tyr1545Cys
ENST00000414678.8:c.4703A>G	ENSP00000412835.3:p.Tyr1568Cys
ENST00000637015.2:c.4922A>G	ENSP00000489729.2:p.Tyr1641Cys
ENST00000346085.10:c.4673A>G	ENSP00000344546.5:p.Tyr1558Cys
ENST00000350026.10:c.4385A>G	ENSP00000055163.7:p.Tyr1462Cys
ENST00000414678.7:c.2951A>G	ENSP00000412835.2:p.Tyr984Cys
ENST00000635849.1:c.2114A>G	ENSP00000490948.1:p.Tyr705Cys
ENST00000635957.1:c.1745A>G	ENSP00000490385.1:p.Tyr582Cys
ENST00000636227.1:n.3256A>G
ENST00000636254.1:n.713A>G
ENST00000636930.2:c.4793A>G MANE Select	ENSP00000490491.2:p.Tyr1598Cys
ENST00000636940.1:n.2790A>G
ENST00000637015.1:c.2161A>G
ENST00000637568.1:c.2075A>G
ENST00000637741.1:n.1459A>G
ENST00000637810.1:c.2135A>G	ENSP00000489636.1:p.Tyr712Cys
ENST00000637904.1:c.2294A>G	ENSP00000490550.1:p.Tyr765Cys
ENST00000647938.1:c.4424A>G	ENSP00000498155.1:p.Tyr1475Cys
ENST00000346085.9:c.4424A>G	ENSP00000344546.4:p.Tyr1475Cys
ENST00000350026.9:c.4385A>G	ENSP00000055163.7:p.Tyr1462Cys
ENST00000414678.6:c.2951A>G	ENSP00000412835.2:p.Tyr984Cys
NM_017519.2:c.4385A>G	NP_059989.2:p.Tyr1462Cys
NM_020732.3:c.4424A>G	NP_065783.3:p.Tyr1475Cys
XM_005267069.3:c.4544A>G	XP_005267126.2:p.Tyr1515Cys
XM_011535984.1:c.3623A>G	XP_011534286.1:p.Tyr1208Cys
XM_011535985.1:c.3443A>G	XP_011534287.1:p.Tyr1148Cys
XM_011535986.1:c.3203A>G	XP_011534288.1:p.Tyr1068Cys
XM_011535987.1:c.2822A>G	XP_011534289.1:p.Tyr941Cys
XM_011535988.1:c.1685A>G	XP_011534290.1:p.Tyr562Cys
NM_001346813.1:c.4544A>G	NP_001333742.1:p.Tyr1515Cys
NM_001363725.1:c.2294A>G	NP_001350654.1:p.Tyr765Cys
XM_011535984.2:c.4754A>G	XP_011534286.2:p.Tyr1585Cys
XM_011535988.3:c.1685A>G	XP_011534290.1:p.Tyr562Cys
XM_017011103.2:c.4655A>G	XP_016866592.1:p.Tyr1552Cys
XM_017011104.1:c.4625A>G	XP_016866593.1:p.Tyr1542Cys
XM_017011105.2:c.4595A>G	XP_016866594.1:p.Tyr1532Cys
XM_017011106.2:c.4466A>G	XP_016866595.1:p.Tyr1489Cys
XM_017011107.2:c.4445A>G	XP_016866596.1:p.Tyr1482Cys
XR_002956289.1:n.4740A>G
NM_001363725.2:c.2294A>G	NP_001350654.1:p.Tyr765Cys
NM_001371656.1:c.4673A>G	NP_001358585.1:p.Tyr1558Cys
NM_001374820.1:c.4673A>G	NP_001361749.1:p.Tyr1558Cys
NM_001374828.1:c.4793A>G MANE Select	NP_001361757.1:p.Tyr1598Cys
NM_017519.3:c.4634A>G	NP_059989.3:p.Tyr1545Cys