Canonical Allele Identifier: CA366227423

Gene: ARID1B

Linked Data

• dbSNP Id: rs1554231196
• MyVariant Identifiers: chr6:g.157502169G>T (hg19) ; chr6:g.157181035G>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3412G>T	ENSP00000055163.8:p.Glu1138Ter
ENST00000414678.8:c.3481G>T	ENSP00000412835.3:p.Glu1161Ter
ENST00000637015.2:c.3700G>T	ENSP00000489729.2:p.Glu1234Ter
ENST00000319584.11:c.1585G>T	ENSP00000313006.7:p.Glu529Ter
ENST00000346085.10:c.3451G>T	ENSP00000344546.5:p.Glu1151Ter
ENST00000350026.10:c.3163G>T	ENSP00000055163.7:p.Glu1055Ter
ENST00000414678.7:c.1729G>T	ENSP00000412835.2:p.Glu577Ter
ENST00000635849.1:c.892G>T	ENSP00000490948.1:p.Glu298Ter
ENST00000635957.1:c.526G>T	ENSP00000490385.1:p.Glu176Ter
ENST00000636930.2:c.3571G>T MANE Select	ENSP00000490491.2:p.Glu1191Ter
ENST00000636940.1:n.1568G>T
ENST00000637015.1:c.939G>T
ENST00000637568.1:c.853G>T
ENST00000637741.1:n.237G>T
ENST00000637810.1:c.913G>T	ENSP00000489636.1:p.Glu305Ter
ENST00000637904.1:c.1072G>T	ENSP00000490550.1:p.Glu358Ter
ENST00000647938.1:c.3202G>T	ENSP00000498155.1:p.Glu1068Ter
ENST00000319584.10:c.1588G>T	ENSP00000313006.6:p.Glu530Ter
ENST00000346085.9:c.3202G>T	ENSP00000344546.4:p.Glu1068Ter
ENST00000350026.9:c.3163G>T	ENSP00000055163.7:p.Glu1055Ter
ENST00000400790.3:c.364G>T	ENSP00000383596.3:p.Glu122Ter
ENST00000414678.6:c.1729G>T	ENSP00000412835.2:p.Glu577Ter
ENST00000478761.3:c.773G>T
NM_017519.2:c.3163G>T	NP_059989.2:p.Glu1055Ter
NM_020732.3:c.3202G>T	NP_065783.3:p.Glu1068Ter
XM_005267069.3:c.3322G>T	XP_005267126.2:p.Glu1108Ter
XM_011535984.1:c.2401G>T	XP_011534286.1:p.Glu801Ter
XM_011535985.1:c.2221G>T	XP_011534287.1:p.Glu741Ter
XM_011535986.1:c.1981G>T	XP_011534288.1:p.Glu661Ter
XM_011535987.1:c.1600G>T	XP_011534289.1:p.Glu534Ter
XM_011535988.1:c.463G>T	XP_011534290.1:p.Glu155Ter
NM_001346813.1:c.3322G>T	NP_001333742.1:p.Glu1108Ter
NM_001363725.1:c.1072G>T	NP_001350654.1:p.Glu358Ter
XM_011535984.2:c.3532G>T	XP_011534286.2:p.Glu1178Ter
XM_011535988.3:c.463G>T	XP_011534290.1:p.Glu155Ter
XM_017011103.2:c.3433G>T	XP_016866592.1:p.Glu1145Ter
XM_017011104.1:c.3403G>T	XP_016866593.1:p.Glu1135Ter
XM_017011105.2:c.3373G>T	XP_016866594.1:p.Glu1125Ter
XM_017011106.2:c.3244G>T	XP_016866595.1:p.Glu1082Ter
XM_017011107.2:c.3223G>T	XP_016866596.1:p.Glu1075Ter
XR_002956289.1:n.3615G>T
NM_001363725.2:c.1072G>T	NP_001350654.1:p.Glu358Ter
NM_001371656.1:c.3451G>T	NP_001358585.1:p.Glu1151Ter
NM_001374820.1:c.3451G>T	NP_001361749.1:p.Glu1151Ter
NM_001374828.1:c.3571G>T MANE Select	NP_001361757.1:p.Glu1191Ter
NM_017519.3:c.3412G>T	NP_059989.3:p.Glu1138Ter