Canonical Allele Identifier: CA366242327

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522382A>T (hg19) ; chr6:g.157201248A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201248A>T , CM000668.2:g.157201248A>T	GRCh38
NC_000006.11:g.157522382A>T , CM000668.1:g.157522382A>T	GRCh37
NC_000006.10:g.157564074A>T	NCBI36
NG_032093.1:g.428319A>T
NG_032093.2:g.428319A>T
NG_066624.1:g.430223A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4864A>T	ENSP00000055163.8:p.Arg1622Trp
ENST00000414678.8:c.4933A>T	ENSP00000412835.3:p.Arg1645Trp
ENST00000637015.2:c.5152A>T	ENSP00000489729.2:p.Arg1718Trp
ENST00000346085.10:c.4903A>T	ENSP00000344546.5:p.Arg1635Trp
ENST00000350026.10:c.4615A>T	ENSP00000055163.7:p.Arg1539Trp
ENST00000414678.7:c.3181A>T	ENSP00000412835.2:p.Arg1061Trp
ENST00000635849.1:c.2344A>T	ENSP00000490948.1:p.Arg782Trp
ENST00000635957.1:c.1975A>T	ENSP00000490385.1:p.Arg659Trp
ENST00000636227.1:n.3486A>T
ENST00000636254.1:n.943A>T
ENST00000636930.2:c.5023A>T MANE Select	ENSP00000490491.2:p.Arg1675Trp
ENST00000636940.1:n.3020A>T
ENST00000637015.1:c.2391A>T
ENST00000637568.1:c.2305A>T
ENST00000637741.1:n.1689A>T
ENST00000637810.1:c.2365A>T	ENSP00000489636.1:p.Arg789Trp
ENST00000637904.1:c.2524A>T	ENSP00000490550.1:p.Arg842Trp
ENST00000647938.1:c.4654A>T	ENSP00000498155.1:p.Arg1552Trp
ENST00000346085.9:c.4654A>T	ENSP00000344546.4:p.Arg1552Trp
ENST00000350026.9:c.4615A>T	ENSP00000055163.7:p.Arg1539Trp
ENST00000414678.6:c.3181A>T	ENSP00000412835.2:p.Arg1061Trp
NM_017519.2:c.4615A>T	NP_059989.2:p.Arg1539Trp
NM_020732.3:c.4654A>T	NP_065783.3:p.Arg1552Trp
XM_005267069.3:c.4774A>T	XP_005267126.2:p.Arg1592Trp
XM_011535984.1:c.3853A>T	XP_011534286.1:p.Arg1285Trp
XM_011535985.1:c.3673A>T	XP_011534287.1:p.Arg1225Trp
XM_011535986.1:c.3433A>T	XP_011534288.1:p.Arg1145Trp
XM_011535987.1:c.3052A>T	XP_011534289.1:p.Arg1018Trp
XM_011535988.1:c.1915A>T	XP_011534290.1:p.Arg639Trp
NM_001346813.1:c.4774A>T	NP_001333742.1:p.Arg1592Trp
NM_001363725.1:c.2524A>T	NP_001350654.1:p.Arg842Trp
XM_011535984.2:c.4984A>T	XP_011534286.2:p.Arg1662Trp
XM_011535988.3:c.1915A>T	XP_011534290.1:p.Arg639Trp
XM_017011103.2:c.4885A>T	XP_016866592.1:p.Arg1629Trp
XM_017011104.1:c.4855A>T	XP_016866593.1:p.Arg1619Trp
XM_017011105.2:c.4825A>T	XP_016866594.1:p.Arg1609Trp
XM_017011106.2:c.4696A>T	XP_016866595.1:p.Arg1566Trp
XM_017011107.2:c.4675A>T	XP_016866596.1:p.Arg1559Trp
XR_002956289.1:n.4970A>T
NM_001363725.2:c.2524A>T	NP_001350654.1:p.Arg842Trp
NM_001371656.1:c.4903A>T	NP_001358585.1:p.Arg1635Trp
NM_001374820.1:c.4903A>T	NP_001361749.1:p.Arg1635Trp
NM_001374828.1:c.5023A>T MANE Select	NP_001361757.1:p.Arg1675Trp
NM_017519.3:c.4864A>T	NP_059989.3:p.Arg1622Trp