Canonical Allele Identifier: CA366241147

Gene: ARID1B

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4499A>T	ENSP00000055163.8:p.Glu1500Val
ENST00000414678.8:c.4568A>T	ENSP00000412835.3:p.Glu1523Val
ENST00000637015.2:c.4787A>T	ENSP00000489729.2:p.Glu1596Val
ENST00000346085.10:c.4538A>T	ENSP00000344546.5:p.Glu1513Val
ENST00000350026.10:c.4250A>T	ENSP00000055163.7:p.Glu1417Val
ENST00000414678.7:c.2816A>T	ENSP00000412835.2:p.Glu939Val
ENST00000635849.1:c.1979A>T	ENSP00000490948.1:p.Glu660Val
ENST00000635957.1:c.1610A>T	ENSP00000490385.1:p.Glu537Val
ENST00000636227.1:n.3121A>T
ENST00000636254.1:n.578A>T
ENST00000636930.2:c.4658A>T MANE Select	ENSP00000490491.2:p.Glu1553Val
ENST00000636940.1:n.2655A>T
ENST00000637015.1:c.2026A>T
ENST00000637568.1:c.1940A>T
ENST00000637741.1:n.1324A>T
ENST00000637810.1:c.2000A>T	ENSP00000489636.1:p.Glu667Val
ENST00000637904.1:c.2159A>T	ENSP00000490550.1:p.Glu720Val
ENST00000647938.1:c.4289A>T	ENSP00000498155.1:p.Glu1430Val
ENST00000346085.9:c.4289A>T	ENSP00000344546.4:p.Glu1430Val
ENST00000350026.9:c.4250A>T	ENSP00000055163.7:p.Glu1417Val
ENST00000414678.6:c.2816A>T	ENSP00000412835.2:p.Glu939Val
NM_017519.2:c.4250A>T	NP_059989.2:p.Glu1417Val
NM_020732.3:c.4289A>T	NP_065783.3:p.Glu1430Val
XM_005267069.3:c.4409A>T	XP_005267126.2:p.Glu1470Val
XM_011535984.1:c.3488A>T	XP_011534286.1:p.Glu1163Val
XM_011535985.1:c.3308A>T	XP_011534287.1:p.Glu1103Val
XM_011535986.1:c.3068A>T	XP_011534288.1:p.Glu1023Val
XM_011535987.1:c.2687A>T	XP_011534289.1:p.Glu896Val
XM_011535988.1:c.1550A>T	XP_011534290.1:p.Glu517Val
NM_001346813.1:c.4409A>T	NP_001333742.1:p.Glu1470Val
NM_001363725.1:c.2159A>T	NP_001350654.1:p.Glu720Val
XM_011535984.2:c.4619A>T	XP_011534286.2:p.Glu1540Val
XM_011535988.3:c.1550A>T	XP_011534290.1:p.Glu517Val
XM_017011103.2:c.4520A>T	XP_016866592.1:p.Glu1507Val
XM_017011104.1:c.4490A>T	XP_016866593.1:p.Glu1497Val
XM_017011105.2:c.4460A>T	XP_016866594.1:p.Glu1487Val
XM_017011106.2:c.4331A>T	XP_016866595.1:p.Glu1444Val
XM_017011107.2:c.4310A>T	XP_016866596.1:p.Glu1437Val
XR_002956289.1:n.4605A>T
NM_001363725.2:c.2159A>T	NP_001350654.1:p.Glu720Val
NM_001371656.1:c.4538A>T	NP_001358585.1:p.Glu1513Val
NM_001374820.1:c.4538A>T	NP_001361749.1:p.Glu1513Val
NM_001374828.1:c.4658A>T MANE Select	NP_001361757.1:p.Glu1553Val
NM_017519.3:c.4499A>T	NP_059989.3:p.Glu1500Val