Canonical Allele Identifier: CA452780749

Gene: ARID1B

Linked Data

• gnomAD v4: 6-157181031-G-A
• MyVariant Identifiers: chr6:g.157502165G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181031G>A , CM000668.2:g.157181031G>A	GRCh38
NC_000006.11:g.157502165G>A , CM000668.1:g.157502165G>A	GRCh37
NC_000006.10:g.157543857G>A	NCBI36
NG_032093.1:g.408102G>A
NG_032093.2:g.408102G>A
NG_066624.1:g.410006G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3408G>A	ENSP00000055163.8:p.Glu1136=
ENST00000414678.8:c.3477G>A	ENSP00000412835.3:p.Glu1159=
ENST00000637015.2:c.3696G>A	ENSP00000489729.2:p.Glu1232=
ENST00000319584.11:c.1581G>A	ENSP00000313006.7:p.Glu527=
ENST00000346085.10:c.3447G>A	ENSP00000344546.5:p.Glu1149=
ENST00000350026.10:c.3159G>A	ENSP00000055163.7:p.Glu1053=
ENST00000414678.7:c.1725G>A	ENSP00000412835.2:p.Glu575=
ENST00000635849.1:c.888G>A	ENSP00000490948.1:p.Glu296=
ENST00000635957.1:c.522G>A	ENSP00000490385.1:p.Glu174=
ENST00000636930.2:c.3567G>A MANE Select	ENSP00000490491.2:p.Glu1189=
ENST00000636940.1:n.1564G>A
ENST00000637015.1:c.935G>A
ENST00000637568.1:c.849G>A
ENST00000637741.1:n.233G>A
ENST00000637810.1:c.909G>A	ENSP00000489636.1:p.Glu303=
ENST00000637904.1:c.1068G>A	ENSP00000490550.1:p.Glu356=
ENST00000647938.1:c.3198G>A	ENSP00000498155.1:p.Glu1066=
ENST00000319584.10:c.1584G>A	ENSP00000313006.6:p.Glu528=
ENST00000346085.9:c.3198G>A	ENSP00000344546.4:p.Glu1066=
ENST00000350026.9:c.3159G>A	ENSP00000055163.7:p.Glu1053=
ENST00000400790.3:c.360G>A	ENSP00000383596.3:p.Glu120=
ENST00000414678.6:c.1725G>A	ENSP00000412835.2:p.Glu575=
ENST00000478761.3:c.769G>A
NM_017519.2:c.3159G>A	NP_059989.2:p.Glu1053=
NM_020732.3:c.3198G>A	NP_065783.3:p.Glu1066=
XM_005267069.3:c.3318G>A	XP_005267126.2:p.Glu1106=
XM_011535984.1:c.2397G>A	XP_011534286.1:p.Glu799=
XM_011535985.1:c.2217G>A	XP_011534287.1:p.Glu739=
XM_011535986.1:c.1977G>A	XP_011534288.1:p.Glu659=
XM_011535987.1:c.1596G>A	XP_011534289.1:p.Glu532=
XM_011535988.1:c.459G>A	XP_011534290.1:p.Glu153=
NM_001346813.1:c.3318G>A	NP_001333742.1:p.Glu1106=
NM_001363725.1:c.1068G>A	NP_001350654.1:p.Glu356=
XM_011535984.2:c.3528G>A	XP_011534286.2:p.Glu1176=
XM_011535988.3:c.459G>A	XP_011534290.1:p.Glu153=
XM_017011103.2:c.3429G>A	XP_016866592.1:p.Glu1143=
XM_017011104.1:c.3399G>A	XP_016866593.1:p.Glu1133=
XM_017011105.2:c.3369G>A	XP_016866594.1:p.Glu1123=
XM_017011106.2:c.3240G>A	XP_016866595.1:p.Glu1080=
XM_017011107.2:c.3219G>A	XP_016866596.1:p.Glu1073=
XR_002956289.1:n.3611G>A
NM_001363725.2:c.1068G>A	NP_001350654.1:p.Glu356=
NM_001371656.1:c.3447G>A	NP_001358585.1:p.Glu1149=
NM_001374820.1:c.3447G>A	NP_001361749.1:p.Glu1149=
NM_001374828.1:c.3567G>A MANE Select	NP_001361757.1:p.Glu1189=
NM_017519.3:c.3408G>A	NP_059989.3:p.Glu1136=