Canonical Allele Identifier: CA366242743

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522496T>A (hg19) ; chr6:g.157201362T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201362T>A , CM000668.2:g.157201362T>A	GRCh38
NC_000006.11:g.157522496T>A , CM000668.1:g.157522496T>A	GRCh37
NC_000006.10:g.157564188T>A	NCBI36
NG_032093.1:g.428433T>A
NG_032093.2:g.428433T>A
NG_066624.1:g.430337T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4978T>A	ENSP00000055163.8:p.Ser1660Thr
ENST00000414678.8:c.5047T>A	ENSP00000412835.3:p.Ser1683Thr
ENST00000637015.2:c.5266T>A	ENSP00000489729.2:p.Ser1756Thr
ENST00000346085.10:c.5017T>A	ENSP00000344546.5:p.Ser1673Thr
ENST00000350026.10:c.4729T>A	ENSP00000055163.7:p.Ser1577Thr
ENST00000414678.7:c.3295T>A	ENSP00000412835.2:p.Ser1099Thr
ENST00000635849.1:c.2458T>A	ENSP00000490948.1:p.Ser820Thr
ENST00000635957.1:c.2089T>A	ENSP00000490385.1:p.Ser697Thr
ENST00000636227.1:n.3600T>A
ENST00000636254.1:n.1057T>A
ENST00000636930.2:c.5137T>A MANE Select	ENSP00000490491.2:p.Ser1713Thr
ENST00000636940.1:n.3134T>A
ENST00000637015.1:c.2505T>A
ENST00000637568.1:c.2419T>A
ENST00000637741.1:n.1803T>A
ENST00000637810.1:c.2479T>A	ENSP00000489636.1:p.Ser827Thr
ENST00000637904.1:c.2638T>A	ENSP00000490550.1:p.Ser880Thr
ENST00000647938.1:c.4768T>A	ENSP00000498155.1:p.Ser1590Thr
ENST00000346085.9:c.4768T>A	ENSP00000344546.4:p.Ser1590Thr
ENST00000350026.9:c.4729T>A	ENSP00000055163.7:p.Ser1577Thr
ENST00000414678.6:c.3295T>A	ENSP00000412835.2:p.Ser1099Thr
NM_017519.2:c.4729T>A	NP_059989.2:p.Ser1577Thr
NM_020732.3:c.4768T>A	NP_065783.3:p.Ser1590Thr
XM_005267069.3:c.4888T>A	XP_005267126.2:p.Ser1630Thr
XM_011535984.1:c.3967T>A	XP_011534286.1:p.Ser1323Thr
XM_011535985.1:c.3787T>A	XP_011534287.1:p.Ser1263Thr
XM_011535986.1:c.3547T>A	XP_011534288.1:p.Ser1183Thr
XM_011535987.1:c.3166T>A	XP_011534289.1:p.Ser1056Thr
XM_011535988.1:c.2029T>A	XP_011534290.1:p.Ser677Thr
NM_001346813.1:c.4888T>A	NP_001333742.1:p.Ser1630Thr
NM_001363725.1:c.2638T>A	NP_001350654.1:p.Ser880Thr
XM_011535984.2:c.5098T>A	XP_011534286.2:p.Ser1700Thr
XM_011535988.3:c.2029T>A	XP_011534290.1:p.Ser677Thr
XM_017011103.2:c.4999T>A	XP_016866592.1:p.Ser1667Thr
XM_017011104.1:c.4969T>A	XP_016866593.1:p.Ser1657Thr
XM_017011105.2:c.4939T>A	XP_016866594.1:p.Ser1647Thr
XM_017011106.2:c.4810T>A	XP_016866595.1:p.Ser1604Thr
XM_017011107.2:c.4789T>A	XP_016866596.1:p.Ser1597Thr
XR_002956289.1:n.5084T>A
NM_001363725.2:c.2638T>A	NP_001350654.1:p.Ser880Thr
NM_001371656.1:c.5017T>A	NP_001358585.1:p.Ser1673Thr
NM_001374820.1:c.5017T>A	NP_001361749.1:p.Ser1673Thr
NM_001374828.1:c.5137T>A MANE Select	NP_001361757.1:p.Ser1713Thr
NM_017519.3:c.4978T>A	NP_059989.3:p.Ser1660Thr