Canonical Allele Identifier: CA366242246

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522343T>A (hg19) ; chr6:g.157201209T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201209T>A , CM000668.2:g.157201209T>A	GRCh38
NC_000006.11:g.157522343T>A , CM000668.1:g.157522343T>A	GRCh37
NC_000006.10:g.157564035T>A	NCBI36
NG_032093.1:g.428280T>A
NG_032093.2:g.428280T>A
NG_066624.1:g.430184T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4825T>A	ENSP00000055163.8:p.Ser1609Thr
ENST00000414678.8:c.4894T>A	ENSP00000412835.3:p.Ser1632Thr
ENST00000637015.2:c.5113T>A	ENSP00000489729.2:p.Ser1705Thr
ENST00000346085.10:c.4864T>A	ENSP00000344546.5:p.Ser1622Thr
ENST00000350026.10:c.4576T>A	ENSP00000055163.7:p.Ser1526Thr
ENST00000414678.7:c.3142T>A	ENSP00000412835.2:p.Ser1048Thr
ENST00000635849.1:c.2305T>A	ENSP00000490948.1:p.Ser769Thr
ENST00000635957.1:c.1936T>A	ENSP00000490385.1:p.Ser646Thr
ENST00000636227.1:n.3447T>A
ENST00000636254.1:n.904T>A
ENST00000636930.2:c.4984T>A MANE Select	ENSP00000490491.2:p.Ser1662Thr
ENST00000636940.1:n.2981T>A
ENST00000637015.1:c.2352T>A
ENST00000637568.1:c.2266T>A
ENST00000637741.1:n.1650T>A
ENST00000637810.1:c.2326T>A	ENSP00000489636.1:p.Ser776Thr
ENST00000637904.1:c.2485T>A	ENSP00000490550.1:p.Ser829Thr
ENST00000647938.1:c.4615T>A	ENSP00000498155.1:p.Ser1539Thr
ENST00000346085.9:c.4615T>A	ENSP00000344546.4:p.Ser1539Thr
ENST00000350026.9:c.4576T>A	ENSP00000055163.7:p.Ser1526Thr
ENST00000414678.6:c.3142T>A	ENSP00000412835.2:p.Ser1048Thr
NM_017519.2:c.4576T>A	NP_059989.2:p.Ser1526Thr
NM_020732.3:c.4615T>A	NP_065783.3:p.Ser1539Thr
XM_005267069.3:c.4735T>A	XP_005267126.2:p.Ser1579Thr
XM_011535984.1:c.3814T>A	XP_011534286.1:p.Ser1272Thr
XM_011535985.1:c.3634T>A	XP_011534287.1:p.Ser1212Thr
XM_011535986.1:c.3394T>A	XP_011534288.1:p.Ser1132Thr
XM_011535987.1:c.3013T>A	XP_011534289.1:p.Ser1005Thr
XM_011535988.1:c.1876T>A	XP_011534290.1:p.Ser626Thr
NM_001346813.1:c.4735T>A	NP_001333742.1:p.Ser1579Thr
NM_001363725.1:c.2485T>A	NP_001350654.1:p.Ser829Thr
XM_011535984.2:c.4945T>A	XP_011534286.2:p.Ser1649Thr
XM_011535988.3:c.1876T>A	XP_011534290.1:p.Ser626Thr
XM_017011103.2:c.4846T>A	XP_016866592.1:p.Ser1616Thr
XM_017011104.1:c.4816T>A	XP_016866593.1:p.Ser1606Thr
XM_017011105.2:c.4786T>A	XP_016866594.1:p.Ser1596Thr
XM_017011106.2:c.4657T>A	XP_016866595.1:p.Ser1553Thr
XM_017011107.2:c.4636T>A	XP_016866596.1:p.Ser1546Thr
XR_002956289.1:n.4931T>A
NM_001363725.2:c.2485T>A	NP_001350654.1:p.Ser829Thr
NM_001371656.1:c.4864T>A	NP_001358585.1:p.Ser1622Thr
NM_001374820.1:c.4864T>A	NP_001361749.1:p.Ser1622Thr
NM_001374828.1:c.4984T>A MANE Select	NP_001361757.1:p.Ser1662Thr
NM_017519.3:c.4825T>A	NP_059989.3:p.Ser1609Thr