Canonical Allele Identifier: CA366241536

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522154C>G (hg19) ; chr6:g.157201020C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201020C>G , CM000668.2:g.157201020C>G	GRCh38
NC_000006.11:g.157522154C>G , CM000668.1:g.157522154C>G	GRCh37
NC_000006.10:g.157563846C>G	NCBI36
NG_032093.1:g.428091C>G
NG_032093.2:g.428091C>G
NG_066624.1:g.429995C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4636C>G	ENSP00000055163.8:p.Gln1546Glu
ENST00000414678.8:c.4705C>G	ENSP00000412835.3:p.Gln1569Glu
ENST00000637015.2:c.4924C>G	ENSP00000489729.2:p.Gln1642Glu
ENST00000346085.10:c.4675C>G	ENSP00000344546.5:p.Gln1559Glu
ENST00000350026.10:c.4387C>G	ENSP00000055163.7:p.Gln1463Glu
ENST00000414678.7:c.2953C>G	ENSP00000412835.2:p.Gln985Glu
ENST00000635849.1:c.2116C>G	ENSP00000490948.1:p.Gln706Glu
ENST00000635957.1:c.1747C>G	ENSP00000490385.1:p.Gln583Glu
ENST00000636227.1:n.3258C>G
ENST00000636254.1:n.715C>G
ENST00000636930.2:c.4795C>G MANE Select	ENSP00000490491.2:p.Gln1599Glu
ENST00000636940.1:n.2792C>G
ENST00000637015.1:c.2163C>G
ENST00000637568.1:c.2077C>G
ENST00000637741.1:n.1461C>G
ENST00000637810.1:c.2137C>G	ENSP00000489636.1:p.Gln713Glu
ENST00000637904.1:c.2296C>G	ENSP00000490550.1:p.Gln766Glu
ENST00000647938.1:c.4426C>G	ENSP00000498155.1:p.Gln1476Glu
ENST00000346085.9:c.4426C>G	ENSP00000344546.4:p.Gln1476Glu
ENST00000350026.9:c.4387C>G	ENSP00000055163.7:p.Gln1463Glu
ENST00000414678.6:c.2953C>G	ENSP00000412835.2:p.Gln985Glu
NM_017519.2:c.4387C>G	NP_059989.2:p.Gln1463Glu
NM_020732.3:c.4426C>G	NP_065783.3:p.Gln1476Glu
XM_005267069.3:c.4546C>G	XP_005267126.2:p.Gln1516Glu
XM_011535984.1:c.3625C>G	XP_011534286.1:p.Gln1209Glu
XM_011535985.1:c.3445C>G	XP_011534287.1:p.Gln1149Glu
XM_011535986.1:c.3205C>G	XP_011534288.1:p.Gln1069Glu
XM_011535987.1:c.2824C>G	XP_011534289.1:p.Gln942Glu
XM_011535988.1:c.1687C>G	XP_011534290.1:p.Gln563Glu
NM_001346813.1:c.4546C>G	NP_001333742.1:p.Gln1516Glu
NM_001363725.1:c.2296C>G	NP_001350654.1:p.Gln766Glu
XM_011535984.2:c.4756C>G	XP_011534286.2:p.Gln1586Glu
XM_011535988.3:c.1687C>G	XP_011534290.1:p.Gln563Glu
XM_017011103.2:c.4657C>G	XP_016866592.1:p.Gln1553Glu
XM_017011104.1:c.4627C>G	XP_016866593.1:p.Gln1543Glu
XM_017011105.2:c.4597C>G	XP_016866594.1:p.Gln1533Glu
XM_017011106.2:c.4468C>G	XP_016866595.1:p.Gln1490Glu
XM_017011107.2:c.4447C>G	XP_016866596.1:p.Gln1483Glu
XR_002956289.1:n.4742C>G
NM_001363725.2:c.2296C>G	NP_001350654.1:p.Gln766Glu
NM_001371656.1:c.4675C>G	NP_001358585.1:p.Gln1559Glu
NM_001374820.1:c.4675C>G	NP_001361749.1:p.Gln1559Glu
NM_001374828.1:c.4795C>G MANE Select	NP_001361757.1:p.Gln1599Glu
NM_017519.3:c.4636C>G	NP_059989.3:p.Gln1546Glu