Canonical Allele Identifier: CA366241710

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522185A>C (hg19) ; chr6:g.157201051A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201051A>C , CM000668.2:g.157201051A>C	GRCh38
NC_000006.11:g.157522185A>C , CM000668.1:g.157522185A>C	GRCh37
NC_000006.10:g.157563877A>C	NCBI36
NG_032093.1:g.428122A>C
NG_032093.2:g.428122A>C
NG_066624.1:g.430026A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4667A>C	ENSP00000055163.8:p.Gln1556Pro
ENST00000414678.8:c.4736A>C	ENSP00000412835.3:p.Gln1579Pro
ENST00000637015.2:c.4955A>C	ENSP00000489729.2:p.Gln1652Pro
ENST00000346085.10:c.4706A>C	ENSP00000344546.5:p.Gln1569Pro
ENST00000350026.10:c.4418A>C	ENSP00000055163.7:p.Gln1473Pro
ENST00000414678.7:c.2984A>C	ENSP00000412835.2:p.Gln995Pro
ENST00000635849.1:c.2147A>C	ENSP00000490948.1:p.Gln716Pro
ENST00000635957.1:c.1778A>C	ENSP00000490385.1:p.Gln593Pro
ENST00000636227.1:n.3289A>C
ENST00000636254.1:n.746A>C
ENST00000636930.2:c.4826A>C MANE Select	ENSP00000490491.2:p.Gln1609Pro
ENST00000636940.1:n.2823A>C
ENST00000637015.1:c.2194A>C
ENST00000637568.1:c.2108A>C
ENST00000637741.1:n.1492A>C
ENST00000637810.1:c.2168A>C	ENSP00000489636.1:p.Gln723Pro
ENST00000637904.1:c.2327A>C	ENSP00000490550.1:p.Gln776Pro
ENST00000647938.1:c.4457A>C	ENSP00000498155.1:p.Gln1486Pro
ENST00000346085.9:c.4457A>C	ENSP00000344546.4:p.Gln1486Pro
ENST00000350026.9:c.4418A>C	ENSP00000055163.7:p.Gln1473Pro
ENST00000414678.6:c.2984A>C	ENSP00000412835.2:p.Gln995Pro
NM_017519.2:c.4418A>C	NP_059989.2:p.Gln1473Pro
NM_020732.3:c.4457A>C	NP_065783.3:p.Gln1486Pro
XM_005267069.3:c.4577A>C	XP_005267126.2:p.Gln1526Pro
XM_011535984.1:c.3656A>C	XP_011534286.1:p.Gln1219Pro
XM_011535985.1:c.3476A>C	XP_011534287.1:p.Gln1159Pro
XM_011535986.1:c.3236A>C	XP_011534288.1:p.Gln1079Pro
XM_011535987.1:c.2855A>C	XP_011534289.1:p.Gln952Pro
XM_011535988.1:c.1718A>C	XP_011534290.1:p.Gln573Pro
NM_001346813.1:c.4577A>C	NP_001333742.1:p.Gln1526Pro
NM_001363725.1:c.2327A>C	NP_001350654.1:p.Gln776Pro
XM_011535984.2:c.4787A>C	XP_011534286.2:p.Gln1596Pro
XM_011535988.3:c.1718A>C	XP_011534290.1:p.Gln573Pro
XM_017011103.2:c.4688A>C	XP_016866592.1:p.Gln1563Pro
XM_017011104.1:c.4658A>C	XP_016866593.1:p.Gln1553Pro
XM_017011105.2:c.4628A>C	XP_016866594.1:p.Gln1543Pro
XM_017011106.2:c.4499A>C	XP_016866595.1:p.Gln1500Pro
XM_017011107.2:c.4478A>C	XP_016866596.1:p.Gln1493Pro
XR_002956289.1:n.4773A>C
NM_001363725.2:c.2327A>C	NP_001350654.1:p.Gln776Pro
NM_001371656.1:c.4706A>C	NP_001358585.1:p.Gln1569Pro
NM_001374820.1:c.4706A>C	NP_001361749.1:p.Gln1569Pro
NM_001374828.1:c.4826A>C MANE Select	NP_001361757.1:p.Gln1609Pro
NM_017519.3:c.4667A>C	NP_059989.3:p.Gln1556Pro