Canonical Allele Identifier: CA366241908

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522220G>T (hg19) ; chr6:g.157201086G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201086G>T , CM000668.2:g.157201086G>T	GRCh38
NC_000006.11:g.157522220G>T , CM000668.1:g.157522220G>T	GRCh37
NC_000006.10:g.157563912G>T	NCBI36
NG_032093.1:g.428157G>T
NG_032093.2:g.428157G>T
NG_066624.1:g.430061G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4702G>T	ENSP00000055163.8:p.Asp1568Tyr
ENST00000414678.8:c.4771G>T	ENSP00000412835.3:p.Asp1591Tyr
ENST00000637015.2:c.4990G>T	ENSP00000489729.2:p.Asp1664Tyr
ENST00000346085.10:c.4741G>T	ENSP00000344546.5:p.Asp1581Tyr
ENST00000350026.10:c.4453G>T	ENSP00000055163.7:p.Asp1485Tyr
ENST00000414678.7:c.3019G>T	ENSP00000412835.2:p.Asp1007Tyr
ENST00000635849.1:c.2182G>T	ENSP00000490948.1:p.Asp728Tyr
ENST00000635957.1:c.1813G>T	ENSP00000490385.1:p.Asp605Tyr
ENST00000636227.1:n.3324G>T
ENST00000636254.1:n.781G>T
ENST00000636930.2:c.4861G>T MANE Select	ENSP00000490491.2:p.Asp1621Tyr
ENST00000636940.1:n.2858G>T
ENST00000637015.1:c.2229G>T
ENST00000637568.1:c.2143G>T
ENST00000637741.1:n.1527G>T
ENST00000637810.1:c.2203G>T	ENSP00000489636.1:p.Asp735Tyr
ENST00000637904.1:c.2362G>T	ENSP00000490550.1:p.Asp788Tyr
ENST00000647938.1:c.4492G>T	ENSP00000498155.1:p.Asp1498Tyr
ENST00000346085.9:c.4492G>T	ENSP00000344546.4:p.Asp1498Tyr
ENST00000350026.9:c.4453G>T	ENSP00000055163.7:p.Asp1485Tyr
ENST00000414678.6:c.3019G>T	ENSP00000412835.2:p.Asp1007Tyr
NM_017519.2:c.4453G>T	NP_059989.2:p.Asp1485Tyr
NM_020732.3:c.4492G>T	NP_065783.3:p.Asp1498Tyr
XM_005267069.3:c.4612G>T	XP_005267126.2:p.Asp1538Tyr
XM_011535984.1:c.3691G>T	XP_011534286.1:p.Asp1231Tyr
XM_011535985.1:c.3511G>T	XP_011534287.1:p.Asp1171Tyr
XM_011535986.1:c.3271G>T	XP_011534288.1:p.Asp1091Tyr
XM_011535987.1:c.2890G>T	XP_011534289.1:p.Asp964Tyr
XM_011535988.1:c.1753G>T	XP_011534290.1:p.Asp585Tyr
NM_001346813.1:c.4612G>T	NP_001333742.1:p.Asp1538Tyr
NM_001363725.1:c.2362G>T	NP_001350654.1:p.Asp788Tyr
XM_011535984.2:c.4822G>T	XP_011534286.2:p.Asp1608Tyr
XM_011535988.3:c.1753G>T	XP_011534290.1:p.Asp585Tyr
XM_017011103.2:c.4723G>T	XP_016866592.1:p.Asp1575Tyr
XM_017011104.1:c.4693G>T	XP_016866593.1:p.Asp1565Tyr
XM_017011105.2:c.4663G>T	XP_016866594.1:p.Asp1555Tyr
XM_017011106.2:c.4534G>T	XP_016866595.1:p.Asp1512Tyr
XM_017011107.2:c.4513G>T	XP_016866596.1:p.Asp1505Tyr
XR_002956289.1:n.4808G>T
NM_001363725.2:c.2362G>T	NP_001350654.1:p.Asp788Tyr
NM_001371656.1:c.4741G>T	NP_001358585.1:p.Asp1581Tyr
NM_001374820.1:c.4741G>T	NP_001361749.1:p.Asp1581Tyr
NM_001374828.1:c.4861G>T MANE Select	NP_001361757.1:p.Asp1621Tyr
NM_017519.3:c.4702G>T	NP_059989.3:p.Asp1568Tyr