Canonical Allele Identifier: CA366241577

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522160A>G (hg19) ; chr6:g.157201026A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201026A>G , CM000668.2:g.157201026A>G	GRCh38
NC_000006.11:g.157522160A>G , CM000668.1:g.157522160A>G	GRCh37
NC_000006.10:g.157563852A>G	NCBI36
NG_032093.1:g.428097A>G
NG_032093.2:g.428097A>G
NG_066624.1:g.430001A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4642A>G	ENSP00000055163.8:p.Arg1548Gly
ENST00000414678.8:c.4711A>G	ENSP00000412835.3:p.Arg1571Gly
ENST00000637015.2:c.4930A>G	ENSP00000489729.2:p.Arg1644Gly
ENST00000346085.10:c.4681A>G	ENSP00000344546.5:p.Arg1561Gly
ENST00000350026.10:c.4393A>G	ENSP00000055163.7:p.Arg1465Gly
ENST00000414678.7:c.2959A>G	ENSP00000412835.2:p.Arg987Gly
ENST00000635849.1:c.2122A>G	ENSP00000490948.1:p.Arg708Gly
ENST00000635957.1:c.1753A>G	ENSP00000490385.1:p.Arg585Gly
ENST00000636227.1:n.3264A>G
ENST00000636254.1:n.721A>G
ENST00000636930.2:c.4801A>G MANE Select	ENSP00000490491.2:p.Arg1601Gly
ENST00000636940.1:n.2798A>G
ENST00000637015.1:c.2169A>G
ENST00000637568.1:c.2083A>G
ENST00000637741.1:n.1467A>G
ENST00000637810.1:c.2143A>G	ENSP00000489636.1:p.Arg715Gly
ENST00000637904.1:c.2302A>G	ENSP00000490550.1:p.Arg768Gly
ENST00000647938.1:c.4432A>G	ENSP00000498155.1:p.Arg1478Gly
ENST00000346085.9:c.4432A>G	ENSP00000344546.4:p.Arg1478Gly
ENST00000350026.9:c.4393A>G	ENSP00000055163.7:p.Arg1465Gly
ENST00000414678.6:c.2959A>G	ENSP00000412835.2:p.Arg987Gly
NM_017519.2:c.4393A>G	NP_059989.2:p.Arg1465Gly
NM_020732.3:c.4432A>G	NP_065783.3:p.Arg1478Gly
XM_005267069.3:c.4552A>G	XP_005267126.2:p.Arg1518Gly
XM_011535984.1:c.3631A>G	XP_011534286.1:p.Arg1211Gly
XM_011535985.1:c.3451A>G	XP_011534287.1:p.Arg1151Gly
XM_011535986.1:c.3211A>G	XP_011534288.1:p.Arg1071Gly
XM_011535987.1:c.2830A>G	XP_011534289.1:p.Arg944Gly
XM_011535988.1:c.1693A>G	XP_011534290.1:p.Arg565Gly
NM_001346813.1:c.4552A>G	NP_001333742.1:p.Arg1518Gly
NM_001363725.1:c.2302A>G	NP_001350654.1:p.Arg768Gly
XM_011535984.2:c.4762A>G	XP_011534286.2:p.Arg1588Gly
XM_011535988.3:c.1693A>G	XP_011534290.1:p.Arg565Gly
XM_017011103.2:c.4663A>G	XP_016866592.1:p.Arg1555Gly
XM_017011104.1:c.4633A>G	XP_016866593.1:p.Arg1545Gly
XM_017011105.2:c.4603A>G	XP_016866594.1:p.Arg1535Gly
XM_017011106.2:c.4474A>G	XP_016866595.1:p.Arg1492Gly
XM_017011107.2:c.4453A>G	XP_016866596.1:p.Arg1485Gly
XR_002956289.1:n.4748A>G
NM_001363725.2:c.2302A>G	NP_001350654.1:p.Arg768Gly
NM_001371656.1:c.4681A>G	NP_001358585.1:p.Arg1561Gly
NM_001374820.1:c.4681A>G	NP_001361749.1:p.Arg1561Gly
NM_001374828.1:c.4801A>G MANE Select	NP_001361757.1:p.Arg1601Gly
NM_017519.3:c.4642A>G	NP_059989.3:p.Arg1548Gly