Canonical Allele Identifier: CA366242735

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522494C>A (hg19) ; chr6:g.157201360C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201360C>A , CM000668.2:g.157201360C>A	GRCh38
NC_000006.11:g.157522494C>A , CM000668.1:g.157522494C>A	GRCh37
NC_000006.10:g.157564186C>A	NCBI36
NG_032093.1:g.428431C>A
NG_032093.2:g.428431C>A
NG_066624.1:g.430335C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4976C>A	ENSP00000055163.8:p.Thr1659Lys
ENST00000414678.8:c.5045C>A	ENSP00000412835.3:p.Thr1682Lys
ENST00000637015.2:c.5264C>A	ENSP00000489729.2:p.Thr1755Lys
ENST00000346085.10:c.5015C>A	ENSP00000344546.5:p.Thr1672Lys
ENST00000350026.10:c.4727C>A	ENSP00000055163.7:p.Thr1576Lys
ENST00000414678.7:c.3293C>A	ENSP00000412835.2:p.Thr1098Lys
ENST00000635849.1:c.2456C>A	ENSP00000490948.1:p.Thr819Lys
ENST00000635957.1:c.2087C>A	ENSP00000490385.1:p.Thr696Lys
ENST00000636227.1:n.3598C>A
ENST00000636254.1:n.1055C>A
ENST00000636930.2:c.5135C>A MANE Select	ENSP00000490491.2:p.Thr1712Lys
ENST00000636940.1:n.3132C>A
ENST00000637015.1:c.2503C>A
ENST00000637568.1:c.2417C>A
ENST00000637741.1:n.1801C>A
ENST00000637810.1:c.2477C>A	ENSP00000489636.1:p.Thr826Lys
ENST00000637904.1:c.2636C>A	ENSP00000490550.1:p.Thr879Lys
ENST00000647938.1:c.4766C>A	ENSP00000498155.1:p.Thr1589Lys
ENST00000346085.9:c.4766C>A	ENSP00000344546.4:p.Thr1589Lys
ENST00000350026.9:c.4727C>A	ENSP00000055163.7:p.Thr1576Lys
ENST00000414678.6:c.3293C>A	ENSP00000412835.2:p.Thr1098Lys
NM_017519.2:c.4727C>A	NP_059989.2:p.Thr1576Lys
NM_020732.3:c.4766C>A	NP_065783.3:p.Thr1589Lys
XM_005267069.3:c.4886C>A	XP_005267126.2:p.Thr1629Lys
XM_011535984.1:c.3965C>A	XP_011534286.1:p.Thr1322Lys
XM_011535985.1:c.3785C>A	XP_011534287.1:p.Thr1262Lys
XM_011535986.1:c.3545C>A	XP_011534288.1:p.Thr1182Lys
XM_011535987.1:c.3164C>A	XP_011534289.1:p.Thr1055Lys
XM_011535988.1:c.2027C>A	XP_011534290.1:p.Thr676Lys
NM_001346813.1:c.4886C>A	NP_001333742.1:p.Thr1629Lys
NM_001363725.1:c.2636C>A	NP_001350654.1:p.Thr879Lys
XM_011535984.2:c.5096C>A	XP_011534286.2:p.Thr1699Lys
XM_011535988.3:c.2027C>A	XP_011534290.1:p.Thr676Lys
XM_017011103.2:c.4997C>A	XP_016866592.1:p.Thr1666Lys
XM_017011104.1:c.4967C>A	XP_016866593.1:p.Thr1656Lys
XM_017011105.2:c.4937C>A	XP_016866594.1:p.Thr1646Lys
XM_017011106.2:c.4808C>A	XP_016866595.1:p.Thr1603Lys
XM_017011107.2:c.4787C>A	XP_016866596.1:p.Thr1596Lys
XR_002956289.1:n.5082C>A
NM_001363725.2:c.2636C>A	NP_001350654.1:p.Thr879Lys
NM_001371656.1:c.5015C>A	NP_001358585.1:p.Thr1672Lys
NM_001374820.1:c.5015C>A	NP_001361749.1:p.Thr1672Lys
NM_001374828.1:c.5135C>A MANE Select	NP_001361757.1:p.Thr1712Lys
NM_017519.3:c.4976C>A	NP_059989.3:p.Thr1659Lys