Canonical Allele Identifier: CA366241146

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522017A>G (hg19) ; chr6:g.157200883A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200883A>G , CM000668.2:g.157200883A>G	GRCh38
NC_000006.11:g.157522017A>G , CM000668.1:g.157522017A>G	GRCh37
NC_000006.10:g.157563709A>G	NCBI36
NG_032093.1:g.427954A>G
NG_032093.2:g.427954A>G
NG_066624.1:g.429858A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4499A>G	ENSP00000055163.8:p.Glu1500Gly
ENST00000414678.8:c.4568A>G	ENSP00000412835.3:p.Glu1523Gly
ENST00000637015.2:c.4787A>G	ENSP00000489729.2:p.Glu1596Gly
ENST00000346085.10:c.4538A>G	ENSP00000344546.5:p.Glu1513Gly
ENST00000350026.10:c.4250A>G	ENSP00000055163.7:p.Glu1417Gly
ENST00000414678.7:c.2816A>G	ENSP00000412835.2:p.Glu939Gly
ENST00000635849.1:c.1979A>G	ENSP00000490948.1:p.Glu660Gly
ENST00000635957.1:c.1610A>G	ENSP00000490385.1:p.Glu537Gly
ENST00000636227.1:n.3121A>G
ENST00000636254.1:n.578A>G
ENST00000636930.2:c.4658A>G MANE Select	ENSP00000490491.2:p.Glu1553Gly
ENST00000636940.1:n.2655A>G
ENST00000637015.1:c.2026A>G
ENST00000637568.1:c.1940A>G
ENST00000637741.1:n.1324A>G
ENST00000637810.1:c.2000A>G	ENSP00000489636.1:p.Glu667Gly
ENST00000637904.1:c.2159A>G	ENSP00000490550.1:p.Glu720Gly
ENST00000647938.1:c.4289A>G	ENSP00000498155.1:p.Glu1430Gly
ENST00000346085.9:c.4289A>G	ENSP00000344546.4:p.Glu1430Gly
ENST00000350026.9:c.4250A>G	ENSP00000055163.7:p.Glu1417Gly
ENST00000414678.6:c.2816A>G	ENSP00000412835.2:p.Glu939Gly
NM_017519.2:c.4250A>G	NP_059989.2:p.Glu1417Gly
NM_020732.3:c.4289A>G	NP_065783.3:p.Glu1430Gly
XM_005267069.3:c.4409A>G	XP_005267126.2:p.Glu1470Gly
XM_011535984.1:c.3488A>G	XP_011534286.1:p.Glu1163Gly
XM_011535985.1:c.3308A>G	XP_011534287.1:p.Glu1103Gly
XM_011535986.1:c.3068A>G	XP_011534288.1:p.Glu1023Gly
XM_011535987.1:c.2687A>G	XP_011534289.1:p.Glu896Gly
XM_011535988.1:c.1550A>G	XP_011534290.1:p.Glu517Gly
NM_001346813.1:c.4409A>G	NP_001333742.1:p.Glu1470Gly
NM_001363725.1:c.2159A>G	NP_001350654.1:p.Glu720Gly
XM_011535984.2:c.4619A>G	XP_011534286.2:p.Glu1540Gly
XM_011535988.3:c.1550A>G	XP_011534290.1:p.Glu517Gly
XM_017011103.2:c.4520A>G	XP_016866592.1:p.Glu1507Gly
XM_017011104.1:c.4490A>G	XP_016866593.1:p.Glu1497Gly
XM_017011105.2:c.4460A>G	XP_016866594.1:p.Glu1487Gly
XM_017011106.2:c.4331A>G	XP_016866595.1:p.Glu1444Gly
XM_017011107.2:c.4310A>G	XP_016866596.1:p.Glu1437Gly
XR_002956289.1:n.4605A>G
NM_001363725.2:c.2159A>G	NP_001350654.1:p.Glu720Gly
NM_001371656.1:c.4538A>G	NP_001358585.1:p.Glu1513Gly
NM_001374820.1:c.4538A>G	NP_001361749.1:p.Glu1513Gly
NM_001374828.1:c.4658A>G MANE Select	NP_001361757.1:p.Glu1553Gly
NM_017519.3:c.4499A>G	NP_059989.3:p.Glu1500Gly