Canonical Allele Identifier: CA366241867

Gene: ARID1B

Linked Data

• dbSNP Id: rs1794073478
• MyVariant Identifiers: chr6:g.157522212G>T (hg19) ; chr6:g.157201078G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201078G>T , CM000668.2:g.157201078G>T	GRCh38
NC_000006.11:g.157522212G>T , CM000668.1:g.157522212G>T	GRCh37
NC_000006.10:g.157563904G>T	NCBI36
NG_032093.1:g.428149G>T
NG_032093.2:g.428149G>T
NG_066624.1:g.430053G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4694G>T	ENSP00000055163.8:p.Arg1565Leu
ENST00000414678.8:c.4763G>T	ENSP00000412835.3:p.Arg1588Leu
ENST00000637015.2:c.4982G>T	ENSP00000489729.2:p.Arg1661Leu
ENST00000346085.10:c.4733G>T	ENSP00000344546.5:p.Arg1578Leu
ENST00000350026.10:c.4445G>T	ENSP00000055163.7:p.Arg1482Leu
ENST00000414678.7:c.3011G>T	ENSP00000412835.2:p.Arg1004Leu
ENST00000635849.1:c.2174G>T	ENSP00000490948.1:p.Arg725Leu
ENST00000635957.1:c.1805G>T	ENSP00000490385.1:p.Arg602Leu
ENST00000636227.1:n.3316G>T
ENST00000636254.1:n.773G>T
ENST00000636930.2:c.4853G>T MANE Select	ENSP00000490491.2:p.Arg1618Leu
ENST00000636940.1:n.2850G>T
ENST00000637015.1:c.2221G>T
ENST00000637568.1:c.2135G>T
ENST00000637741.1:n.1519G>T
ENST00000637810.1:c.2195G>T	ENSP00000489636.1:p.Arg732Leu
ENST00000637904.1:c.2354G>T	ENSP00000490550.1:p.Arg785Leu
ENST00000647938.1:c.4484G>T	ENSP00000498155.1:p.Arg1495Leu
ENST00000346085.9:c.4484G>T	ENSP00000344546.4:p.Arg1495Leu
ENST00000350026.9:c.4445G>T	ENSP00000055163.7:p.Arg1482Leu
ENST00000414678.6:c.3011G>T	ENSP00000412835.2:p.Arg1004Leu
NM_017519.2:c.4445G>T	NP_059989.2:p.Arg1482Leu
NM_020732.3:c.4484G>T	NP_065783.3:p.Arg1495Leu
XM_005267069.3:c.4604G>T	XP_005267126.2:p.Arg1535Leu
XM_011535984.1:c.3683G>T	XP_011534286.1:p.Arg1228Leu
XM_011535985.1:c.3503G>T	XP_011534287.1:p.Arg1168Leu
XM_011535986.1:c.3263G>T	XP_011534288.1:p.Arg1088Leu
XM_011535987.1:c.2882G>T	XP_011534289.1:p.Arg961Leu
XM_011535988.1:c.1745G>T	XP_011534290.1:p.Arg582Leu
NM_001346813.1:c.4604G>T	NP_001333742.1:p.Arg1535Leu
NM_001363725.1:c.2354G>T	NP_001350654.1:p.Arg785Leu
XM_011535984.2:c.4814G>T	XP_011534286.2:p.Arg1605Leu
XM_011535988.3:c.1745G>T	XP_011534290.1:p.Arg582Leu
XM_017011103.2:c.4715G>T	XP_016866592.1:p.Arg1572Leu
XM_017011104.1:c.4685G>T	XP_016866593.1:p.Arg1562Leu
XM_017011105.2:c.4655G>T	XP_016866594.1:p.Arg1552Leu
XM_017011106.2:c.4526G>T	XP_016866595.1:p.Arg1509Leu
XM_017011107.2:c.4505G>T	XP_016866596.1:p.Arg1502Leu
XR_002956289.1:n.4800G>T
NM_001363725.2:c.2354G>T	NP_001350654.1:p.Arg785Leu
NM_001371656.1:c.4733G>T	NP_001358585.1:p.Arg1578Leu
NM_001374820.1:c.4733G>T	NP_001361749.1:p.Arg1578Leu
NM_001374828.1:c.4853G>T MANE Select	NP_001361757.1:p.Arg1618Leu
NM_017519.3:c.4694G>T	NP_059989.3:p.Arg1565Leu