Canonical Allele Identifier: CA366234283

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510895A>G (hg19) ; chr6:g.157189761A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189761A>G , CM000668.2:g.157189761A>G	GRCh38
NC_000006.11:g.157510895A>G , CM000668.1:g.157510895A>G	GRCh37
NC_000006.10:g.157552587A>G	NCBI36
NG_032093.1:g.416832A>G
NG_032093.2:g.416832A>G
NG_066624.1:g.418736A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3880A>G	ENSP00000055163.8:p.Thr1294Ala
ENST00000414678.8:c.3949A>G	ENSP00000412835.3:p.Thr1317Ala
ENST00000637015.2:c.4168A>G	ENSP00000489729.2:p.Thr1390Ala
ENST00000346085.10:c.3919A>G	ENSP00000344546.5:p.Thr1307Ala
ENST00000350026.10:c.3631A>G	ENSP00000055163.7:p.Thr1211Ala
ENST00000414678.7:c.2197A>G	ENSP00000412835.2:p.Thr733Ala
ENST00000635849.1:c.1360A>G	ENSP00000490948.1:p.Thr454Ala
ENST00000635957.1:c.994A>G	ENSP00000490385.1:p.Thr332Ala
ENST00000636930.2:c.4039A>G MANE Select	ENSP00000490491.2:p.Thr1347Ala
ENST00000636940.1:n.2036A>G
ENST00000637015.1:c.1407A>G
ENST00000637568.1:c.1321A>G
ENST00000637741.1:n.705A>G
ENST00000637810.1:c.1381A>G	ENSP00000489636.1:p.Thr461Ala
ENST00000637904.1:c.1540A>G	ENSP00000490550.1:p.Thr514Ala
ENST00000647938.1:c.3670A>G	ENSP00000498155.1:p.Thr1224Ala
ENST00000346085.9:c.3670A>G	ENSP00000344546.4:p.Thr1224Ala
ENST00000350026.9:c.3631A>G	ENSP00000055163.7:p.Thr1211Ala
ENST00000414678.6:c.2197A>G	ENSP00000412835.2:p.Thr733Ala
NM_017519.2:c.3631A>G	NP_059989.2:p.Thr1211Ala
NM_020732.3:c.3670A>G	NP_065783.3:p.Thr1224Ala
XM_005267069.3:c.3790A>G	XP_005267126.2:p.Thr1264Ala
XM_011535984.1:c.2869A>G	XP_011534286.1:p.Thr957Ala
XM_011535985.1:c.2689A>G	XP_011534287.1:p.Thr897Ala
XM_011535986.1:c.2449A>G	XP_011534288.1:p.Thr817Ala
XM_011535987.1:c.2068A>G	XP_011534289.1:p.Thr690Ala
XM_011535988.1:c.931A>G	XP_011534290.1:p.Thr311Ala
NM_001346813.1:c.3790A>G	NP_001333742.1:p.Thr1264Ala
NM_001363725.1:c.1540A>G	NP_001350654.1:p.Thr514Ala
XM_011535984.2:c.4000A>G	XP_011534286.2:p.Thr1334Ala
XM_011535988.3:c.931A>G	XP_011534290.1:p.Thr311Ala
XM_017011103.2:c.3901A>G	XP_016866592.1:p.Thr1301Ala
XM_017011104.1:c.3871A>G	XP_016866593.1:p.Thr1291Ala
XM_017011105.2:c.3841A>G	XP_016866594.1:p.Thr1281Ala
XM_017011106.2:c.3712A>G	XP_016866595.1:p.Thr1238Ala
XM_017011107.2:c.3691A>G	XP_016866596.1:p.Thr1231Ala
XR_002956289.1:n.4083A>G
NM_001363725.2:c.1540A>G	NP_001350654.1:p.Thr514Ala
NM_001371656.1:c.3919A>G	NP_001358585.1:p.Thr1307Ala
NM_001374820.1:c.3919A>G	NP_001361749.1:p.Thr1307Ala
NM_001374828.1:c.4039A>G MANE Select	NP_001361757.1:p.Thr1347Ala
NM_017519.3:c.3880A>G	NP_059989.3:p.Thr1294Ala