Canonical Allele Identifier: CA366239557

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157519963G>T (hg19) ; chr6:g.157198829G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157198829G>T , CM000668.2:g.157198829G>T	GRCh38
NC_000006.11:g.157519963G>T , CM000668.1:g.157519963G>T	GRCh37
NC_000006.10:g.157561655G>T	NCBI36
NG_032093.1:g.425900G>T
NG_032093.2:g.425900G>T
NG_066624.1:g.427804G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4242G>T	ENSP00000055163.8:p.Gln1414His
ENST00000414678.8:c.4311G>T	ENSP00000412835.3:p.Gln1437His
ENST00000637015.2:c.4530G>T	ENSP00000489729.2:p.Gln1510His
ENST00000346085.10:c.4281G>T	ENSP00000344546.5:p.Gln1427His
ENST00000350026.10:c.3993G>T	ENSP00000055163.7:p.Gln1331His
ENST00000414678.7:c.2559G>T	ENSP00000412835.2:p.Gln853His
ENST00000635849.1:c.1722G>T	ENSP00000490948.1:p.Gln574His
ENST00000635957.1:c.1353G>T	ENSP00000490385.1:p.Gln451His
ENST00000636227.1:n.2864G>T
ENST00000636254.1:n.321G>T
ENST00000636930.2:c.4401G>T MANE Select	ENSP00000490491.2:p.Gln1467His
ENST00000636940.1:n.2398G>T
ENST00000637015.1:c.1769G>T
ENST00000637568.1:c.1683G>T
ENST00000637741.1:n.1067G>T
ENST00000637810.1:c.1743G>T	ENSP00000489636.1:p.Gln581His
ENST00000637904.1:c.1902G>T	ENSP00000490550.1:p.Gln634His
ENST00000647938.1:c.4032G>T	ENSP00000498155.1:p.Gln1344His
ENST00000346085.9:c.4032G>T	ENSP00000344546.4:p.Gln1344His
ENST00000350026.9:c.3993G>T	ENSP00000055163.7:p.Gln1331His
ENST00000414678.6:c.2559G>T	ENSP00000412835.2:p.Gln853His
NM_017519.2:c.3993G>T	NP_059989.2:p.Gln1331His
NM_020732.3:c.4032G>T	NP_065783.3:p.Gln1344His
XM_005267069.3:c.4152G>T	XP_005267126.2:p.Gln1384His
XM_011535984.1:c.3231G>T	XP_011534286.1:p.Gln1077His
XM_011535985.1:c.3051G>T	XP_011534287.1:p.Gln1017His
XM_011535986.1:c.2811G>T	XP_011534288.1:p.Gln937His
XM_011535987.1:c.2430G>T	XP_011534289.1:p.Gln810His
XM_011535988.1:c.1293G>T	XP_011534290.1:p.Gln431His
NM_001346813.1:c.4152G>T	NP_001333742.1:p.Gln1384His
NM_001363725.1:c.1902G>T	NP_001350654.1:p.Gln634His
XM_011535984.2:c.4362G>T	XP_011534286.2:p.Gln1454His
XM_011535988.3:c.1293G>T	XP_011534290.1:p.Gln431His
XM_017011103.2:c.4263G>T	XP_016866592.1:p.Gln1421His
XM_017011104.1:c.4233G>T	XP_016866593.1:p.Gln1411His
XM_017011105.2:c.4203G>T	XP_016866594.1:p.Gln1401His
XM_017011106.2:c.4074G>T	XP_016866595.1:p.Gln1358His
XM_017011107.2:c.4053G>T	XP_016866596.1:p.Gln1351His
XR_002956289.1:n.4427-1876G>T
NM_001363725.2:c.1902G>T	NP_001350654.1:p.Gln634His
NM_001371656.1:c.4281G>T	NP_001358585.1:p.Gln1427His
NM_001374820.1:c.4281G>T	NP_001361749.1:p.Gln1427His
NM_001374828.1:c.4401G>T MANE Select	NP_001361757.1:p.Gln1467His
NM_017519.3:c.4242G>T	NP_059989.3:p.Gln1414His