Canonical Allele Identifier: CA366227418

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157502169G>A (hg19) ; chr6:g.157181035G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181035G>A , CM000668.2:g.157181035G>A	GRCh38
NC_000006.11:g.157502169G>A , CM000668.1:g.157502169G>A	GRCh37
NC_000006.10:g.157543861G>A	NCBI36
NG_032093.1:g.408106G>A
NG_032093.2:g.408106G>A
NG_066624.1:g.410010G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3412G>A	ENSP00000055163.8:p.Glu1138Lys
ENST00000414678.8:c.3481G>A	ENSP00000412835.3:p.Glu1161Lys
ENST00000637015.2:c.3700G>A	ENSP00000489729.2:p.Glu1234Lys
ENST00000319584.11:c.1585G>A	ENSP00000313006.7:p.Glu529Lys
ENST00000346085.10:c.3451G>A	ENSP00000344546.5:p.Glu1151Lys
ENST00000350026.10:c.3163G>A	ENSP00000055163.7:p.Glu1055Lys
ENST00000414678.7:c.1729G>A	ENSP00000412835.2:p.Glu577Lys
ENST00000635849.1:c.892G>A	ENSP00000490948.1:p.Glu298Lys
ENST00000635957.1:c.526G>A	ENSP00000490385.1:p.Glu176Lys
ENST00000636930.2:c.3571G>A MANE Select	ENSP00000490491.2:p.Glu1191Lys
ENST00000636940.1:n.1568G>A
ENST00000637015.1:c.939G>A
ENST00000637568.1:c.853G>A
ENST00000637741.1:n.237G>A
ENST00000637810.1:c.913G>A	ENSP00000489636.1:p.Glu305Lys
ENST00000637904.1:c.1072G>A	ENSP00000490550.1:p.Glu358Lys
ENST00000647938.1:c.3202G>A	ENSP00000498155.1:p.Glu1068Lys
ENST00000319584.10:c.1588G>A	ENSP00000313006.6:p.Glu530Lys
ENST00000346085.9:c.3202G>A	ENSP00000344546.4:p.Glu1068Lys
ENST00000350026.9:c.3163G>A	ENSP00000055163.7:p.Glu1055Lys
ENST00000400790.3:c.364G>A	ENSP00000383596.3:p.Glu122Lys
ENST00000414678.6:c.1729G>A	ENSP00000412835.2:p.Glu577Lys
ENST00000478761.3:c.773G>A
NM_017519.2:c.3163G>A	NP_059989.2:p.Glu1055Lys
NM_020732.3:c.3202G>A	NP_065783.3:p.Glu1068Lys
XM_005267069.3:c.3322G>A	XP_005267126.2:p.Glu1108Lys
XM_011535984.1:c.2401G>A	XP_011534286.1:p.Glu801Lys
XM_011535985.1:c.2221G>A	XP_011534287.1:p.Glu741Lys
XM_011535986.1:c.1981G>A	XP_011534288.1:p.Glu661Lys
XM_011535987.1:c.1600G>A	XP_011534289.1:p.Glu534Lys
XM_011535988.1:c.463G>A	XP_011534290.1:p.Glu155Lys
NM_001346813.1:c.3322G>A	NP_001333742.1:p.Glu1108Lys
NM_001363725.1:c.1072G>A	NP_001350654.1:p.Glu358Lys
XM_011535984.2:c.3532G>A	XP_011534286.2:p.Glu1178Lys
XM_011535988.3:c.463G>A	XP_011534290.1:p.Glu155Lys
XM_017011103.2:c.3433G>A	XP_016866592.1:p.Glu1145Lys
XM_017011104.1:c.3403G>A	XP_016866593.1:p.Glu1135Lys
XM_017011105.2:c.3373G>A	XP_016866594.1:p.Glu1125Lys
XM_017011106.2:c.3244G>A	XP_016866595.1:p.Glu1082Lys
XM_017011107.2:c.3223G>A	XP_016866596.1:p.Glu1075Lys
XR_002956289.1:n.3615G>A
NM_001363725.2:c.1072G>A	NP_001350654.1:p.Glu358Lys
NM_001371656.1:c.3451G>A	NP_001358585.1:p.Glu1151Lys
NM_001374820.1:c.3451G>A	NP_001361749.1:p.Glu1151Lys
NM_001374828.1:c.3571G>A MANE Select	NP_001361757.1:p.Glu1191Lys
NM_017519.3:c.3412G>A	NP_059989.3:p.Glu1138Lys