Canonical Allele Identifier: CA366246198

Gene: ARID1B

Linked Data

• dbSNP Id: rs1554237171
• MyVariant Identifiers: chr6:g.157527523G>A (hg19) ; chr6:g.157206389G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157206389G>A , CM000668.2:g.157206389G>A	GRCh38
NC_000006.11:g.157527523G>A , CM000668.1:g.157527523G>A	GRCh37
NC_000006.10:g.157569215G>A	NCBI36
NG_032093.1:g.433460G>A
NG_032093.2:g.433460G>A
NG_066624.1:g.435364G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.5458G>A	ENSP00000055163.8:p.Glu1820Lys
ENST00000414678.8:c.5527G>A	ENSP00000412835.3:p.Glu1843Lys
ENST00000637015.2:c.5746G>A	ENSP00000489729.2:p.Glu1916Lys
ENST00000346085.10:c.5497G>A	ENSP00000344546.5:p.Glu1833Lys
ENST00000350026.10:c.5209G>A	ENSP00000055163.7:p.Glu1737Lys
ENST00000414678.7:c.3775G>A	ENSP00000412835.2:p.Glu1259Lys
ENST00000635849.1:c.2938G>A	ENSP00000490948.1:p.Glu980Lys
ENST00000635957.1:c.2569G>A	ENSP00000490385.1:p.Glu857Lys
ENST00000636227.1:n.4080G>A
ENST00000636254.1:n.1537G>A
ENST00000636930.2:c.5617G>A MANE Select	ENSP00000490491.2:p.Glu1873Lys
ENST00000636940.1:n.3614G>A
ENST00000637015.1:c.2985G>A
ENST00000637568.1:c.2899G>A
ENST00000637741.1:n.2283G>A
ENST00000637810.1:c.2959G>A	ENSP00000489636.1:p.Glu987Lys
ENST00000637904.1:c.3118G>A	ENSP00000490550.1:p.Glu1040Lys
ENST00000637933.1:n.2732G>A
ENST00000647938.1:c.5248G>A	ENSP00000498155.1:p.Glu1750Lys
ENST00000346085.9:c.5248G>A	ENSP00000344546.4:p.Glu1750Lys
ENST00000350026.9:c.5209G>A	ENSP00000055163.7:p.Glu1737Lys
ENST00000414678.6:c.3775G>A	ENSP00000412835.2:p.Glu1259Lys
NM_017519.2:c.5209G>A	NP_059989.2:p.Glu1737Lys
NM_020732.3:c.5248G>A	NP_065783.3:p.Glu1750Lys
XM_005267069.3:c.5368G>A	XP_005267126.2:p.Glu1790Lys
XM_011535984.1:c.4447G>A	XP_011534286.1:p.Glu1483Lys
XM_011535985.1:c.4267G>A	XP_011534287.1:p.Glu1423Lys
XM_011535986.1:c.4027G>A	XP_011534288.1:p.Glu1343Lys
XM_011535987.1:c.3646G>A	XP_011534289.1:p.Glu1216Lys
XM_011535988.1:c.2509G>A	XP_011534290.1:p.Glu837Lys
NM_001346813.1:c.5368G>A	NP_001333742.1:p.Glu1790Lys
NM_001363725.1:c.3118G>A	NP_001350654.1:p.Glu1040Lys
XM_011535984.2:c.5578G>A	XP_011534286.2:p.Glu1860Lys
XM_011535988.3:c.2509G>A	XP_011534290.1:p.Glu837Lys
XM_017011103.2:c.5479G>A	XP_016866592.1:p.Glu1827Lys
XM_017011104.1:c.5449G>A	XP_016866593.1:p.Glu1817Lys
XM_017011105.2:c.5419G>A	XP_016866594.1:p.Glu1807Lys
XM_017011106.2:c.5290G>A	XP_016866595.1:p.Glu1764Lys
XM_017011107.2:c.5269G>A	XP_016866596.1:p.Glu1757Lys
XR_002956289.1:n.5564G>A
NM_001363725.2:c.3118G>A	NP_001350654.1:p.Glu1040Lys
NM_001371656.1:c.5497G>A	NP_001358585.1:p.Glu1833Lys
NM_001374820.1:c.5497G>A	NP_001361749.1:p.Glu1833Lys
NM_001374828.1:c.5617G>A MANE Select	NP_001361757.1:p.Glu1873Lys
NM_017519.3:c.5458G>A	NP_059989.3:p.Glu1820Lys