Canonical Allele Identifier: CA452978019

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522066G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200932G>A , CM000668.2:g.157200932G>A	GRCh38
NC_000006.11:g.157522066G>A , CM000668.1:g.157522066G>A	GRCh37
NC_000006.10:g.157563758G>A	NCBI36
NG_032093.1:g.428003G>A
NG_032093.2:g.428003G>A
NG_066624.1:g.429907G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4548G>A	ENSP00000055163.8:p.Gln1516=
ENST00000414678.8:c.4617G>A	ENSP00000412835.3:p.Gln1539=
ENST00000637015.2:c.4836G>A	ENSP00000489729.2:p.Gln1612=
ENST00000346085.10:c.4587G>A	ENSP00000344546.5:p.Gln1529=
ENST00000350026.10:c.4299G>A	ENSP00000055163.7:p.Gln1433=
ENST00000414678.7:c.2865G>A	ENSP00000412835.2:p.Gln955=
ENST00000635849.1:c.2028G>A	ENSP00000490948.1:p.Gln676=
ENST00000635957.1:c.1659G>A	ENSP00000490385.1:p.Gln553=
ENST00000636227.1:n.3170G>A
ENST00000636254.1:n.627G>A
ENST00000636930.2:c.4707G>A MANE Select	ENSP00000490491.2:p.Gln1569=
ENST00000636940.1:n.2704G>A
ENST00000637015.1:c.2075G>A
ENST00000637568.1:c.1989G>A
ENST00000637741.1:n.1373G>A
ENST00000637810.1:c.2049G>A	ENSP00000489636.1:p.Gln683=
ENST00000637904.1:c.2208G>A	ENSP00000490550.1:p.Gln736=
ENST00000647938.1:c.4338G>A	ENSP00000498155.1:p.Gln1446=
ENST00000346085.9:c.4338G>A	ENSP00000344546.4:p.Gln1446=
ENST00000350026.9:c.4299G>A	ENSP00000055163.7:p.Gln1433=
ENST00000414678.6:c.2865G>A	ENSP00000412835.2:p.Gln955=
NM_017519.2:c.4299G>A	NP_059989.2:p.Gln1433=
NM_020732.3:c.4338G>A	NP_065783.3:p.Gln1446=
XM_005267069.3:c.4458G>A	XP_005267126.2:p.Gln1486=
XM_011535984.1:c.3537G>A	XP_011534286.1:p.Gln1179=
XM_011535985.1:c.3357G>A	XP_011534287.1:p.Gln1119=
XM_011535986.1:c.3117G>A	XP_011534288.1:p.Gln1039=
XM_011535987.1:c.2736G>A	XP_011534289.1:p.Gln912=
XM_011535988.1:c.1599G>A	XP_011534290.1:p.Gln533=
NM_001346813.1:c.4458G>A	NP_001333742.1:p.Gln1486=
NM_001363725.1:c.2208G>A	NP_001350654.1:p.Gln736=
XM_011535984.2:c.4668G>A	XP_011534286.2:p.Gln1556=
XM_011535988.3:c.1599G>A	XP_011534290.1:p.Gln533=
XM_017011103.2:c.4569G>A	XP_016866592.1:p.Gln1523=
XM_017011104.1:c.4539G>A	XP_016866593.1:p.Gln1513=
XM_017011105.2:c.4509G>A	XP_016866594.1:p.Gln1503=
XM_017011106.2:c.4380G>A	XP_016866595.1:p.Gln1460=
XM_017011107.2:c.4359G>A	XP_016866596.1:p.Gln1453=
XR_002956289.1:n.4654G>A
NM_001363725.2:c.2208G>A	NP_001350654.1:p.Gln736=
NM_001371656.1:c.4587G>A	NP_001358585.1:p.Gln1529=
NM_001374820.1:c.4587G>A	NP_001361749.1:p.Gln1529=
NM_001374828.1:c.4707G>A MANE Select	NP_001361757.1:p.Gln1569=
NM_017519.3:c.4548G>A	NP_059989.3:p.Gln1516=