Canonical Allele Identifier: CA366234118

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128338822
• gnomAD v4: 6-157189701-G-A
• MyVariant Identifiers: chr6:g.157510835G>A (hg19) ; chr6:g.157189701G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189701G>A , CM000668.2:g.157189701G>A	GRCh38
NC_000006.11:g.157510835G>A , CM000668.1:g.157510835G>A	GRCh37
NC_000006.10:g.157552527G>A	NCBI36
NG_032093.1:g.416772G>A
NG_032093.2:g.416772G>A
NG_066624.1:g.418676G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3820G>A	ENSP00000055163.8:p.Ala1274Thr
ENST00000414678.8:c.3889G>A	ENSP00000412835.3:p.Ala1297Thr
ENST00000637015.2:c.4108G>A	ENSP00000489729.2:p.Ala1370Thr
ENST00000346085.10:c.3859G>A	ENSP00000344546.5:p.Ala1287Thr
ENST00000350026.10:c.3571G>A	ENSP00000055163.7:p.Ala1191Thr
ENST00000414678.7:c.2137G>A	ENSP00000412835.2:p.Ala713Thr
ENST00000635849.1:c.1300G>A	ENSP00000490948.1:p.Ala434Thr
ENST00000635957.1:c.934G>A	ENSP00000490385.1:p.Ala312Thr
ENST00000636930.2:c.3979G>A MANE Select	ENSP00000490491.2:p.Ala1327Thr
ENST00000636940.1:n.1976G>A
ENST00000637015.1:c.1347G>A
ENST00000637568.1:c.1261G>A
ENST00000637741.1:n.645G>A
ENST00000637810.1:c.1321G>A	ENSP00000489636.1:p.Ala441Thr
ENST00000637904.1:c.1480G>A	ENSP00000490550.1:p.Ala494Thr
ENST00000647938.1:c.3610G>A	ENSP00000498155.1:p.Ala1204Thr
ENST00000346085.9:c.3610G>A	ENSP00000344546.4:p.Ala1204Thr
ENST00000350026.9:c.3571G>A	ENSP00000055163.7:p.Ala1191Thr
ENST00000414678.6:c.2137G>A	ENSP00000412835.2:p.Ala713Thr
NM_017519.2:c.3571G>A	NP_059989.2:p.Ala1191Thr
NM_020732.3:c.3610G>A	NP_065783.3:p.Ala1204Thr
XM_005267069.3:c.3730G>A	XP_005267126.2:p.Ala1244Thr
XM_011535984.1:c.2809G>A	XP_011534286.1:p.Ala937Thr
XM_011535985.1:c.2629G>A	XP_011534287.1:p.Ala877Thr
XM_011535986.1:c.2389G>A	XP_011534288.1:p.Ala797Thr
XM_011535987.1:c.2008G>A	XP_011534289.1:p.Ala670Thr
XM_011535988.1:c.871G>A	XP_011534290.1:p.Ala291Thr
NM_001346813.1:c.3730G>A	NP_001333742.1:p.Ala1244Thr
NM_001363725.1:c.1480G>A	NP_001350654.1:p.Ala494Thr
XM_011535984.2:c.3940G>A	XP_011534286.2:p.Ala1314Thr
XM_011535988.3:c.871G>A	XP_011534290.1:p.Ala291Thr
XM_017011103.2:c.3841G>A	XP_016866592.1:p.Ala1281Thr
XM_017011104.1:c.3811G>A	XP_016866593.1:p.Ala1271Thr
XM_017011105.2:c.3781G>A	XP_016866594.1:p.Ala1261Thr
XM_017011106.2:c.3652G>A	XP_016866595.1:p.Ala1218Thr
XM_017011107.2:c.3631G>A	XP_016866596.1:p.Ala1211Thr
XR_002956289.1:n.4023G>A
NM_001363725.2:c.1480G>A	NP_001350654.1:p.Ala494Thr
NM_001371656.1:c.3859G>A	NP_001358585.1:p.Ala1287Thr
NM_001374820.1:c.3859G>A	NP_001361749.1:p.Ala1287Thr
NM_001374828.1:c.3979G>A MANE Select	NP_001361757.1:p.Ala1327Thr
NM_017519.3:c.3820G>A	NP_059989.3:p.Ala1274Thr