Canonical Allele Identifier: CA366227887

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157502215G>T (hg19) ; chr6:g.157181081G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181081G>T , CM000668.2:g.157181081G>T	GRCh38
NC_000006.11:g.157502215G>T , CM000668.1:g.157502215G>T	GRCh37
NC_000006.10:g.157543907G>T	NCBI36
NG_032093.1:g.408152G>T
NG_032093.2:g.408152G>T
NG_066624.1:g.410056G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3458G>T	ENSP00000055163.8:p.Arg1153Ile
ENST00000414678.8:c.3527G>T	ENSP00000412835.3:p.Arg1176Ile
ENST00000637015.2:c.3746G>T	ENSP00000489729.2:p.Arg1249Ile
ENST00000319584.11:c.1631G>T	ENSP00000313006.7:p.Arg544Ile
ENST00000346085.10:c.3497G>T	ENSP00000344546.5:p.Arg1166Ile
ENST00000350026.10:c.3209G>T	ENSP00000055163.7:p.Arg1070Ile
ENST00000414678.7:c.1775G>T	ENSP00000412835.2:p.Arg592Ile
ENST00000635849.1:c.938G>T	ENSP00000490948.1:p.Arg313Ile
ENST00000635957.1:c.572G>T	ENSP00000490385.1:p.Arg191Ile
ENST00000636930.2:c.3617G>T MANE Select	ENSP00000490491.2:p.Arg1206Ile
ENST00000636940.1:n.1614G>T
ENST00000637015.1:c.985G>T
ENST00000637568.1:c.899G>T
ENST00000637741.1:n.283G>T
ENST00000637810.1:c.959G>T	ENSP00000489636.1:p.Arg320Ile
ENST00000637904.1:c.1118G>T	ENSP00000490550.1:p.Arg373Ile
ENST00000647938.1:c.3248G>T	ENSP00000498155.1:p.Arg1083Ile
ENST00000319584.10:c.1634G>T	ENSP00000313006.6:p.Arg545Ile
ENST00000346085.9:c.3248G>T	ENSP00000344546.4:p.Arg1083Ile
ENST00000350026.9:c.3209G>T	ENSP00000055163.7:p.Arg1070Ile
ENST00000400790.3:c.410G>T	ENSP00000383596.3:p.Arg137Ile
ENST00000414678.6:c.1775G>T	ENSP00000412835.2:p.Arg592Ile
ENST00000478761.3:c.819G>T
NM_017519.2:c.3209G>T	NP_059989.2:p.Arg1070Ile
NM_020732.3:c.3248G>T	NP_065783.3:p.Arg1083Ile
XM_005267069.3:c.3368G>T	XP_005267126.2:p.Arg1123Ile
XM_011535984.1:c.2447G>T	XP_011534286.1:p.Arg816Ile
XM_011535985.1:c.2267G>T	XP_011534287.1:p.Arg756Ile
XM_011535986.1:c.2027G>T	XP_011534288.1:p.Arg676Ile
XM_011535987.1:c.1646G>T	XP_011534289.1:p.Arg549Ile
XM_011535988.1:c.509G>T	XP_011534290.1:p.Arg170Ile
NM_001346813.1:c.3368G>T	NP_001333742.1:p.Arg1123Ile
NM_001363725.1:c.1118G>T	NP_001350654.1:p.Arg373Ile
XM_011535984.2:c.3578G>T	XP_011534286.2:p.Arg1193Ile
XM_011535988.3:c.509G>T	XP_011534290.1:p.Arg170Ile
XM_017011103.2:c.3479G>T	XP_016866592.1:p.Arg1160Ile
XM_017011104.1:c.3449G>T	XP_016866593.1:p.Arg1150Ile
XM_017011105.2:c.3419G>T	XP_016866594.1:p.Arg1140Ile
XM_017011106.2:c.3290G>T	XP_016866595.1:p.Arg1097Ile
XM_017011107.2:c.3269G>T	XP_016866596.1:p.Arg1090Ile
XR_002956289.1:n.3661G>T
NM_001363725.2:c.1118G>T	NP_001350654.1:p.Arg373Ile
NM_001371656.1:c.3497G>T	NP_001358585.1:p.Arg1166Ile
NM_001374820.1:c.3497G>T	NP_001361749.1:p.Arg1166Ile
NM_001374828.1:c.3617G>T MANE Select	NP_001361757.1:p.Arg1206Ile
NM_017519.3:c.3458G>T	NP_059989.3:p.Arg1153Ile