Canonical Allele Identifier: CA366241208

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522044A>C (hg19) ; chr6:g.157200910A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200910A>C , CM000668.2:g.157200910A>C	GRCh38
NC_000006.11:g.157522044A>C , CM000668.1:g.157522044A>C	GRCh37
NC_000006.10:g.157563736A>C	NCBI36
NG_032093.1:g.427981A>C
NG_032093.2:g.427981A>C
NG_066624.1:g.429885A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4526A>C	ENSP00000055163.8:p.Gln1509Pro
ENST00000414678.8:c.4595A>C	ENSP00000412835.3:p.Gln1532Pro
ENST00000637015.2:c.4814A>C	ENSP00000489729.2:p.Gln1605Pro
ENST00000346085.10:c.4565A>C	ENSP00000344546.5:p.Gln1522Pro
ENST00000350026.10:c.4277A>C	ENSP00000055163.7:p.Gln1426Pro
ENST00000414678.7:c.2843A>C	ENSP00000412835.2:p.Gln948Pro
ENST00000635849.1:c.2006A>C	ENSP00000490948.1:p.Gln669Pro
ENST00000635957.1:c.1637A>C	ENSP00000490385.1:p.Gln546Pro
ENST00000636227.1:n.3148A>C
ENST00000636254.1:n.605A>C
ENST00000636930.2:c.4685A>C MANE Select	ENSP00000490491.2:p.Gln1562Pro
ENST00000636940.1:n.2682A>C
ENST00000637015.1:c.2053A>C
ENST00000637568.1:c.1967A>C
ENST00000637741.1:n.1351A>C
ENST00000637810.1:c.2027A>C	ENSP00000489636.1:p.Gln676Pro
ENST00000637904.1:c.2186A>C	ENSP00000490550.1:p.Gln729Pro
ENST00000647938.1:c.4316A>C	ENSP00000498155.1:p.Gln1439Pro
ENST00000346085.9:c.4316A>C	ENSP00000344546.4:p.Gln1439Pro
ENST00000350026.9:c.4277A>C	ENSP00000055163.7:p.Gln1426Pro
ENST00000414678.6:c.2843A>C	ENSP00000412835.2:p.Gln948Pro
NM_017519.2:c.4277A>C	NP_059989.2:p.Gln1426Pro
NM_020732.3:c.4316A>C	NP_065783.3:p.Gln1439Pro
XM_005267069.3:c.4436A>C	XP_005267126.2:p.Gln1479Pro
XM_011535984.1:c.3515A>C	XP_011534286.1:p.Gln1172Pro
XM_011535985.1:c.3335A>C	XP_011534287.1:p.Gln1112Pro
XM_011535986.1:c.3095A>C	XP_011534288.1:p.Gln1032Pro
XM_011535987.1:c.2714A>C	XP_011534289.1:p.Gln905Pro
XM_011535988.1:c.1577A>C	XP_011534290.1:p.Gln526Pro
NM_001346813.1:c.4436A>C	NP_001333742.1:p.Gln1479Pro
NM_001363725.1:c.2186A>C	NP_001350654.1:p.Gln729Pro
XM_011535984.2:c.4646A>C	XP_011534286.2:p.Gln1549Pro
XM_011535988.3:c.1577A>C	XP_011534290.1:p.Gln526Pro
XM_017011103.2:c.4547A>C	XP_016866592.1:p.Gln1516Pro
XM_017011104.1:c.4517A>C	XP_016866593.1:p.Gln1506Pro
XM_017011105.2:c.4487A>C	XP_016866594.1:p.Gln1496Pro
XM_017011106.2:c.4358A>C	XP_016866595.1:p.Gln1453Pro
XM_017011107.2:c.4337A>C	XP_016866596.1:p.Gln1446Pro
XR_002956289.1:n.4632A>C
NM_001363725.2:c.2186A>C	NP_001350654.1:p.Gln729Pro
NM_001371656.1:c.4565A>C	NP_001358585.1:p.Gln1522Pro
NM_001374820.1:c.4565A>C	NP_001361749.1:p.Gln1522Pro
NM_001374828.1:c.4685A>C MANE Select	NP_001361757.1:p.Gln1562Pro
NM_017519.3:c.4526A>C	NP_059989.3:p.Gln1509Pro