Canonical Allele Identifier: CA366242773

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128376296
• MyVariant Identifiers: chr6:g.157522502G>A (hg19) ; chr6:g.157201368G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201368G>A , CM000668.2:g.157201368G>A	GRCh38
NC_000006.11:g.157522502G>A , CM000668.1:g.157522502G>A	GRCh37
NC_000006.10:g.157564194G>A	NCBI36
NG_032093.1:g.428439G>A
NG_032093.2:g.428439G>A
NG_066624.1:g.430343G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4984G>A	ENSP00000055163.8:p.Val1662Ile
ENST00000414678.8:c.5053G>A	ENSP00000412835.3:p.Val1685Ile
ENST00000637015.2:c.5272G>A	ENSP00000489729.2:p.Val1758Ile
ENST00000346085.10:c.5023G>A	ENSP00000344546.5:p.Val1675Ile
ENST00000350026.10:c.4735G>A	ENSP00000055163.7:p.Val1579Ile
ENST00000414678.7:c.3301G>A	ENSP00000412835.2:p.Val1101Ile
ENST00000635849.1:c.2464G>A	ENSP00000490948.1:p.Val822Ile
ENST00000635957.1:c.2095G>A	ENSP00000490385.1:p.Val699Ile
ENST00000636227.1:n.3606G>A
ENST00000636254.1:n.1063G>A
ENST00000636930.2:c.5143G>A MANE Select	ENSP00000490491.2:p.Val1715Ile
ENST00000636940.1:n.3140G>A
ENST00000637015.1:c.2511G>A
ENST00000637568.1:c.2425G>A
ENST00000637741.1:n.1809G>A
ENST00000637810.1:c.2485G>A	ENSP00000489636.1:p.Val829Ile
ENST00000637904.1:c.2644G>A	ENSP00000490550.1:p.Val882Ile
ENST00000647938.1:c.4774G>A	ENSP00000498155.1:p.Val1592Ile
ENST00000346085.9:c.4774G>A	ENSP00000344546.4:p.Val1592Ile
ENST00000350026.9:c.4735G>A	ENSP00000055163.7:p.Val1579Ile
ENST00000414678.6:c.3301G>A	ENSP00000412835.2:p.Val1101Ile
NM_017519.2:c.4735G>A	NP_059989.2:p.Val1579Ile
NM_020732.3:c.4774G>A	NP_065783.3:p.Val1592Ile
XM_005267069.3:c.4894G>A	XP_005267126.2:p.Val1632Ile
XM_011535984.1:c.3973G>A	XP_011534286.1:p.Val1325Ile
XM_011535985.1:c.3793G>A	XP_011534287.1:p.Val1265Ile
XM_011535986.1:c.3553G>A	XP_011534288.1:p.Val1185Ile
XM_011535987.1:c.3172G>A	XP_011534289.1:p.Val1058Ile
XM_011535988.1:c.2035G>A	XP_011534290.1:p.Val679Ile
NM_001346813.1:c.4894G>A	NP_001333742.1:p.Val1632Ile
NM_001363725.1:c.2644G>A	NP_001350654.1:p.Val882Ile
XM_011535984.2:c.5104G>A	XP_011534286.2:p.Val1702Ile
XM_011535988.3:c.2035G>A	XP_011534290.1:p.Val679Ile
XM_017011103.2:c.5005G>A	XP_016866592.1:p.Val1669Ile
XM_017011104.1:c.4975G>A	XP_016866593.1:p.Val1659Ile
XM_017011105.2:c.4945G>A	XP_016866594.1:p.Val1649Ile
XM_017011106.2:c.4816G>A	XP_016866595.1:p.Val1606Ile
XM_017011107.2:c.4795G>A	XP_016866596.1:p.Val1599Ile
XR_002956289.1:n.5090G>A
NM_001363725.2:c.2644G>A	NP_001350654.1:p.Val882Ile
NM_001371656.1:c.5023G>A	NP_001358585.1:p.Val1675Ile
NM_001374820.1:c.5023G>A	NP_001361749.1:p.Val1675Ile
NM_001374828.1:c.5143G>A MANE Select	NP_001361757.1:p.Val1715Ile
NM_017519.3:c.4984G>A	NP_059989.3:p.Val1662Ile