Canonical Allele Identifier: CA366241586

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522161G>T (hg19) ; chr6:g.157201027G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201027G>T , CM000668.2:g.157201027G>T	GRCh38
NC_000006.11:g.157522161G>T , CM000668.1:g.157522161G>T	GRCh37
NC_000006.10:g.157563853G>T	NCBI36
NG_032093.1:g.428098G>T
NG_032093.2:g.428098G>T
NG_066624.1:g.430002G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4643G>T	ENSP00000055163.8:p.Arg1548Met
ENST00000414678.8:c.4712G>T	ENSP00000412835.3:p.Arg1571Met
ENST00000637015.2:c.4931G>T	ENSP00000489729.2:p.Arg1644Met
ENST00000346085.10:c.4682G>T	ENSP00000344546.5:p.Arg1561Met
ENST00000350026.10:c.4394G>T	ENSP00000055163.7:p.Arg1465Met
ENST00000414678.7:c.2960G>T	ENSP00000412835.2:p.Arg987Met
ENST00000635849.1:c.2123G>T	ENSP00000490948.1:p.Arg708Met
ENST00000635957.1:c.1754G>T	ENSP00000490385.1:p.Arg585Met
ENST00000636227.1:n.3265G>T
ENST00000636254.1:n.722G>T
ENST00000636930.2:c.4802G>T MANE Select	ENSP00000490491.2:p.Arg1601Met
ENST00000636940.1:n.2799G>T
ENST00000637015.1:c.2170G>T
ENST00000637568.1:c.2084G>T
ENST00000637741.1:n.1468G>T
ENST00000637810.1:c.2144G>T	ENSP00000489636.1:p.Arg715Met
ENST00000637904.1:c.2303G>T	ENSP00000490550.1:p.Arg768Met
ENST00000647938.1:c.4433G>T	ENSP00000498155.1:p.Arg1478Met
ENST00000346085.9:c.4433G>T	ENSP00000344546.4:p.Arg1478Met
ENST00000350026.9:c.4394G>T	ENSP00000055163.7:p.Arg1465Met
ENST00000414678.6:c.2960G>T	ENSP00000412835.2:p.Arg987Met
NM_017519.2:c.4394G>T	NP_059989.2:p.Arg1465Met
NM_020732.3:c.4433G>T	NP_065783.3:p.Arg1478Met
XM_005267069.3:c.4553G>T	XP_005267126.2:p.Arg1518Met
XM_011535984.1:c.3632G>T	XP_011534286.1:p.Arg1211Met
XM_011535985.1:c.3452G>T	XP_011534287.1:p.Arg1151Met
XM_011535986.1:c.3212G>T	XP_011534288.1:p.Arg1071Met
XM_011535987.1:c.2831G>T	XP_011534289.1:p.Arg944Met
XM_011535988.1:c.1694G>T	XP_011534290.1:p.Arg565Met
NM_001346813.1:c.4553G>T	NP_001333742.1:p.Arg1518Met
NM_001363725.1:c.2303G>T	NP_001350654.1:p.Arg768Met
XM_011535984.2:c.4763G>T	XP_011534286.2:p.Arg1588Met
XM_011535988.3:c.1694G>T	XP_011534290.1:p.Arg565Met
XM_017011103.2:c.4664G>T	XP_016866592.1:p.Arg1555Met
XM_017011104.1:c.4634G>T	XP_016866593.1:p.Arg1545Met
XM_017011105.2:c.4604G>T	XP_016866594.1:p.Arg1535Met
XM_017011106.2:c.4475G>T	XP_016866595.1:p.Arg1492Met
XM_017011107.2:c.4454G>T	XP_016866596.1:p.Arg1485Met
XR_002956289.1:n.4749G>T
NM_001363725.2:c.2303G>T	NP_001350654.1:p.Arg768Met
NM_001371656.1:c.4682G>T	NP_001358585.1:p.Arg1561Met
NM_001374820.1:c.4682G>T	NP_001361749.1:p.Arg1561Met
NM_001374828.1:c.4802G>T MANE Select	NP_001361757.1:p.Arg1601Met
NM_017519.3:c.4643G>T	NP_059989.3:p.Arg1548Met