Canonical Allele Identifier: CA452978111

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522285T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201151T>G , CM000668.2:g.157201151T>G	GRCh38
NC_000006.11:g.157522285T>G , CM000668.1:g.157522285T>G	GRCh37
NC_000006.10:g.157563977T>G	NCBI36
NG_032093.1:g.428222T>G
NG_032093.2:g.428222T>G
NG_066624.1:g.430126T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4767T>G	ENSP00000055163.8:p.Arg1589=
ENST00000414678.8:c.4836T>G	ENSP00000412835.3:p.Arg1612=
ENST00000637015.2:c.5055T>G	ENSP00000489729.2:p.Arg1685=
ENST00000346085.10:c.4806T>G	ENSP00000344546.5:p.Arg1602=
ENST00000350026.10:c.4518T>G	ENSP00000055163.7:p.Arg1506=
ENST00000414678.7:c.3084T>G	ENSP00000412835.2:p.Arg1028=
ENST00000635849.1:c.2247T>G	ENSP00000490948.1:p.Arg749=
ENST00000635957.1:c.1878T>G	ENSP00000490385.1:p.Arg626=
ENST00000636227.1:n.3389T>G
ENST00000636254.1:n.846T>G
ENST00000636930.2:c.4926T>G MANE Select	ENSP00000490491.2:p.Arg1642=
ENST00000636940.1:n.2923T>G
ENST00000637015.1:c.2294T>G
ENST00000637568.1:c.2208T>G
ENST00000637741.1:n.1592T>G
ENST00000637810.1:c.2268T>G	ENSP00000489636.1:p.Arg756=
ENST00000637904.1:c.2427T>G	ENSP00000490550.1:p.Arg809=
ENST00000647938.1:c.4557T>G	ENSP00000498155.1:p.Arg1519=
ENST00000346085.9:c.4557T>G	ENSP00000344546.4:p.Arg1519=
ENST00000350026.9:c.4518T>G	ENSP00000055163.7:p.Arg1506=
ENST00000414678.6:c.3084T>G	ENSP00000412835.2:p.Arg1028=
NM_017519.2:c.4518T>G	NP_059989.2:p.Arg1506=
NM_020732.3:c.4557T>G	NP_065783.3:p.Arg1519=
XM_005267069.3:c.4677T>G	XP_005267126.2:p.Arg1559=
XM_011535984.1:c.3756T>G	XP_011534286.1:p.Arg1252=
XM_011535985.1:c.3576T>G	XP_011534287.1:p.Arg1192=
XM_011535986.1:c.3336T>G	XP_011534288.1:p.Arg1112=
XM_011535987.1:c.2955T>G	XP_011534289.1:p.Arg985=
XM_011535988.1:c.1818T>G	XP_011534290.1:p.Arg606=
NM_001346813.1:c.4677T>G	NP_001333742.1:p.Arg1559=
NM_001363725.1:c.2427T>G	NP_001350654.1:p.Arg809=
XM_011535984.2:c.4887T>G	XP_011534286.2:p.Arg1629=
XM_011535988.3:c.1818T>G	XP_011534290.1:p.Arg606=
XM_017011103.2:c.4788T>G	XP_016866592.1:p.Arg1596=
XM_017011104.1:c.4758T>G	XP_016866593.1:p.Arg1586=
XM_017011105.2:c.4728T>G	XP_016866594.1:p.Arg1576=
XM_017011106.2:c.4599T>G	XP_016866595.1:p.Arg1533=
XM_017011107.2:c.4578T>G	XP_016866596.1:p.Arg1526=
XR_002956289.1:n.4873T>G
NM_001363725.2:c.2427T>G	NP_001350654.1:p.Arg809=
NM_001371656.1:c.4806T>G	NP_001358585.1:p.Arg1602=
NM_001374820.1:c.4806T>G	NP_001361749.1:p.Arg1602=
NM_001374828.1:c.4926T>G MANE Select	NP_001361757.1:p.Arg1642=
NM_017519.3:c.4767T>G	NP_059989.3:p.Arg1589=