Canonical Allele Identifier: CA452784767

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522501G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201367G>A , CM000668.2:g.157201367G>A	GRCh38
NC_000006.11:g.157522501G>A , CM000668.1:g.157522501G>A	GRCh37
NC_000006.10:g.157564193G>A	NCBI36
NG_032093.1:g.428438G>A
NG_032093.2:g.428438G>A
NG_066624.1:g.430342G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4983G>A	ENSP00000055163.8:p.Gln1661=
ENST00000414678.8:c.5052G>A	ENSP00000412835.3:p.Gln1684=
ENST00000637015.2:c.5271G>A	ENSP00000489729.2:p.Gln1757=
ENST00000346085.10:c.5022G>A	ENSP00000344546.5:p.Gln1674=
ENST00000350026.10:c.4734G>A	ENSP00000055163.7:p.Gln1578=
ENST00000414678.7:c.3300G>A	ENSP00000412835.2:p.Gln1100=
ENST00000635849.1:c.2463G>A	ENSP00000490948.1:p.Gln821=
ENST00000635957.1:c.2094G>A	ENSP00000490385.1:p.Gln698=
ENST00000636227.1:n.3605G>A
ENST00000636254.1:n.1062G>A
ENST00000636930.2:c.5142G>A MANE Select	ENSP00000490491.2:p.Gln1714=
ENST00000636940.1:n.3139G>A
ENST00000637015.1:c.2510G>A
ENST00000637568.1:c.2424G>A
ENST00000637741.1:n.1808G>A
ENST00000637810.1:c.2484G>A	ENSP00000489636.1:p.Gln828=
ENST00000637904.1:c.2643G>A	ENSP00000490550.1:p.Gln881=
ENST00000647938.1:c.4773G>A	ENSP00000498155.1:p.Gln1591=
ENST00000346085.9:c.4773G>A	ENSP00000344546.4:p.Gln1591=
ENST00000350026.9:c.4734G>A	ENSP00000055163.7:p.Gln1578=
ENST00000414678.6:c.3300G>A	ENSP00000412835.2:p.Gln1100=
NM_017519.2:c.4734G>A	NP_059989.2:p.Gln1578=
NM_020732.3:c.4773G>A	NP_065783.3:p.Gln1591=
XM_005267069.3:c.4893G>A	XP_005267126.2:p.Gln1631=
XM_011535984.1:c.3972G>A	XP_011534286.1:p.Gln1324=
XM_011535985.1:c.3792G>A	XP_011534287.1:p.Gln1264=
XM_011535986.1:c.3552G>A	XP_011534288.1:p.Gln1184=
XM_011535987.1:c.3171G>A	XP_011534289.1:p.Gln1057=
XM_011535988.1:c.2034G>A	XP_011534290.1:p.Gln678=
NM_001346813.1:c.4893G>A	NP_001333742.1:p.Gln1631=
NM_001363725.1:c.2643G>A	NP_001350654.1:p.Gln881=
XM_011535984.2:c.5103G>A	XP_011534286.2:p.Gln1701=
XM_011535988.3:c.2034G>A	XP_011534290.1:p.Gln678=
XM_017011103.2:c.5004G>A	XP_016866592.1:p.Gln1668=
XM_017011104.1:c.4974G>A	XP_016866593.1:p.Gln1658=
XM_017011105.2:c.4944G>A	XP_016866594.1:p.Gln1648=
XM_017011106.2:c.4815G>A	XP_016866595.1:p.Gln1605=
XM_017011107.2:c.4794G>A	XP_016866596.1:p.Gln1598=
XR_002956289.1:n.5089G>A
NM_001363725.2:c.2643G>A	NP_001350654.1:p.Gln881=
NM_001371656.1:c.5022G>A	NP_001358585.1:p.Gln1674=
NM_001374820.1:c.5022G>A	NP_001361749.1:p.Gln1674=
NM_001374828.1:c.5142G>A MANE Select	NP_001361757.1:p.Gln1714=
NM_017519.3:c.4983G>A	NP_059989.3:p.Gln1661=