Canonical Allele Identifier: CA366389296

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157470079A>G (hg19) ; chr6:g.157148945A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148945A>G , CM000668.2:g.157148945A>G	GRCh38
NC_000006.11:g.157470079A>G , CM000668.1:g.157470079A>G	GRCh37
NC_000006.10:g.157511771A>G	NCBI36
NG_032093.1:g.376016A>G
NG_032093.2:g.376016A>G
NG_066624.1:g.377920A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3083A>G	ENSP00000055163.8:p.Gln1028Arg
ENST00000414678.8:c.2993A>G	ENSP00000412835.3:p.Gln998Arg
ENST00000637015.2:c.3083A>G	ENSP00000489729.2:p.Gln1028Arg
ENST00000319584.11:c.1097A>G	ENSP00000313006.7:p.Gln366Arg
ENST00000346085.10:c.3122A>G	ENSP00000344546.5:p.Gln1041Arg
ENST00000350026.10:c.2834A>G	ENSP00000055163.7:p.Gln945Arg
ENST00000414678.7:c.1241A>G	ENSP00000412835.2:p.Gln414Arg
ENST00000452544.2:n.984A>G
ENST00000635849.1:c.404A>G	ENSP00000490948.1:p.Gln135Arg
ENST00000635957.1:c.38A>G	ENSP00000490385.1:p.Gln13Arg
ENST00000636426.1:n.217A>G
ENST00000636930.2:c.3083A>G MANE Select	ENSP00000490491.2:p.Gln1028Arg
ENST00000637015.1:c.322A>G
ENST00000637568.1:c.126A>G
ENST00000637810.1:c.584A>G	ENSP00000489636.1:p.Gln195Arg
ENST00000637904.1:c.584A>G	ENSP00000490550.1:p.Gln195Arg
ENST00000647938.1:c.2873A>G	ENSP00000498155.1:p.Gln958Arg
ENST00000674190.1:n.1832A>G
ENST00000319584.10:c.1100A>G	ENSP00000313006.6:p.Gln367Arg
ENST00000346085.9:c.2873A>G	ENSP00000344546.4:p.Gln958Arg
ENST00000350026.9:c.2834A>G	ENSP00000055163.7:p.Gln945Arg
ENST00000400790.3:c.35A>G	ENSP00000383596.3:p.Gln12Arg
ENST00000414678.6:c.1241A>G	ENSP00000412835.2:p.Gln414Arg
ENST00000452544.1:n.930A>G
ENST00000478761.3:c.156A>G
NM_017519.2:c.2834A>G	NP_059989.2:p.Gln945Arg
NM_020732.3:c.2873A>G	NP_065783.3:p.Gln958Arg
XM_005267069.3:c.2834A>G	XP_005267126.2:p.Gln945Arg
XM_011535984.1:c.1784A>G	XP_011534286.1:p.Gln595Arg
XM_011535985.1:c.1604A>G	XP_011534287.1:p.Gln535Arg
XM_011535986.1:c.1364A>G	XP_011534288.1:p.Gln455Arg
XM_011535987.1:c.983A>G	XP_011534289.1:p.Gln328Arg
XM_011535988.1:c.-20+15738A>G	XP_011534290.1:n.-20+15738A>G
NM_001346813.1:c.2834A>G	NP_001333742.1:p.Gln945Arg
NM_001363725.1:c.584A>G	NP_001350654.1:p.Gln195Arg
XM_011535984.2:c.2915A>G	XP_011534286.2:p.Gln972Arg
XM_011535988.3:c.-20+15738A>G	XP_011534290.1:n.-20+15738A>G
XM_017011103.2:c.2915A>G	XP_016866592.1:p.Gln972Arg
XM_017011104.1:c.2915A>G	XP_016866593.1:p.Gln972Arg
XM_017011105.2:c.2915A>G	XP_016866594.1:p.Gln972Arg
XM_017011106.2:c.2915A>G	XP_016866595.1:p.Gln972Arg
XM_017011107.2:c.2735A>G	XP_016866596.1:p.Gln912Arg
XR_002956289.1:n.2998A>G
NM_001363725.2:c.584A>G	NP_001350654.1:p.Gln195Arg
NM_001371656.1:c.3122A>G	NP_001358585.1:p.Gln1041Arg
NM_001374820.1:c.3122A>G	NP_001361749.1:p.Gln1041Arg
NM_001374828.1:c.3083A>G MANE Select	NP_001361757.1:p.Gln1028Arg
NM_017519.3:c.3083A>G	NP_059989.3:p.Gln1028Arg