Canonical Allele Identifier: CA366242569

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522464A>C (hg19) ; chr6:g.157201330A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201330A>C , CM000668.2:g.157201330A>C	GRCh38
NC_000006.11:g.157522464A>C , CM000668.1:g.157522464A>C	GRCh37
NC_000006.10:g.157564156A>C	NCBI36
NG_032093.1:g.428401A>C
NG_032093.2:g.428401A>C
NG_066624.1:g.430305A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4946A>C	ENSP00000055163.8:p.Lys1649Thr
ENST00000414678.8:c.5015A>C	ENSP00000412835.3:p.Lys1672Thr
ENST00000637015.2:c.5234A>C	ENSP00000489729.2:p.Lys1745Thr
ENST00000346085.10:c.4985A>C	ENSP00000344546.5:p.Lys1662Thr
ENST00000350026.10:c.4697A>C	ENSP00000055163.7:p.Lys1566Thr
ENST00000414678.7:c.3263A>C	ENSP00000412835.2:p.Lys1088Thr
ENST00000635849.1:c.2426A>C	ENSP00000490948.1:p.Lys809Thr
ENST00000635957.1:c.2057A>C	ENSP00000490385.1:p.Lys686Thr
ENST00000636227.1:n.3568A>C
ENST00000636254.1:n.1025A>C
ENST00000636930.2:c.5105A>C MANE Select	ENSP00000490491.2:p.Lys1702Thr
ENST00000636940.1:n.3102A>C
ENST00000637015.1:c.2473A>C
ENST00000637568.1:c.2387A>C
ENST00000637741.1:n.1771A>C
ENST00000637810.1:c.2447A>C	ENSP00000489636.1:p.Lys816Thr
ENST00000637904.1:c.2606A>C	ENSP00000490550.1:p.Lys869Thr
ENST00000647938.1:c.4736A>C	ENSP00000498155.1:p.Lys1579Thr
ENST00000346085.9:c.4736A>C	ENSP00000344546.4:p.Lys1579Thr
ENST00000350026.9:c.4697A>C	ENSP00000055163.7:p.Lys1566Thr
ENST00000414678.6:c.3263A>C	ENSP00000412835.2:p.Lys1088Thr
NM_017519.2:c.4697A>C	NP_059989.2:p.Lys1566Thr
NM_020732.3:c.4736A>C	NP_065783.3:p.Lys1579Thr
XM_005267069.3:c.4856A>C	XP_005267126.2:p.Lys1619Thr
XM_011535984.1:c.3935A>C	XP_011534286.1:p.Lys1312Thr
XM_011535985.1:c.3755A>C	XP_011534287.1:p.Lys1252Thr
XM_011535986.1:c.3515A>C	XP_011534288.1:p.Lys1172Thr
XM_011535987.1:c.3134A>C	XP_011534289.1:p.Lys1045Thr
XM_011535988.1:c.1997A>C	XP_011534290.1:p.Lys666Thr
NM_001346813.1:c.4856A>C	NP_001333742.1:p.Lys1619Thr
NM_001363725.1:c.2606A>C	NP_001350654.1:p.Lys869Thr
XM_011535984.2:c.5066A>C	XP_011534286.2:p.Lys1689Thr
XM_011535988.3:c.1997A>C	XP_011534290.1:p.Lys666Thr
XM_017011103.2:c.4967A>C	XP_016866592.1:p.Lys1656Thr
XM_017011104.1:c.4937A>C	XP_016866593.1:p.Lys1646Thr
XM_017011105.2:c.4907A>C	XP_016866594.1:p.Lys1636Thr
XM_017011106.2:c.4778A>C	XP_016866595.1:p.Lys1593Thr
XM_017011107.2:c.4757A>C	XP_016866596.1:p.Lys1586Thr
XR_002956289.1:n.5052A>C
NM_001363725.2:c.2606A>C	NP_001350654.1:p.Lys869Thr
NM_001371656.1:c.4985A>C	NP_001358585.1:p.Lys1662Thr
NM_001374820.1:c.4985A>C	NP_001361749.1:p.Lys1662Thr
NM_001374828.1:c.5105A>C MANE Select	NP_001361757.1:p.Lys1702Thr
NM_017519.3:c.4946A>C	NP_059989.3:p.Lys1649Thr