Canonical Allele Identifier: CA366234125

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510838G>C (hg19) ; chr6:g.157189704G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189704G>C , CM000668.2:g.157189704G>C	GRCh38
NC_000006.11:g.157510838G>C , CM000668.1:g.157510838G>C	GRCh37
NC_000006.10:g.157552530G>C	NCBI36
NG_032093.1:g.416775G>C
NG_032093.2:g.416775G>C
NG_066624.1:g.418679G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3823G>C	ENSP00000055163.8:p.Glu1275Gln
ENST00000414678.8:c.3892G>C	ENSP00000412835.3:p.Glu1298Gln
ENST00000637015.2:c.4111G>C	ENSP00000489729.2:p.Glu1371Gln
ENST00000346085.10:c.3862G>C	ENSP00000344546.5:p.Glu1288Gln
ENST00000350026.10:c.3574G>C	ENSP00000055163.7:p.Glu1192Gln
ENST00000414678.7:c.2140G>C	ENSP00000412835.2:p.Glu714Gln
ENST00000635849.1:c.1303G>C	ENSP00000490948.1:p.Glu435Gln
ENST00000635957.1:c.937G>C	ENSP00000490385.1:p.Glu313Gln
ENST00000636930.2:c.3982G>C MANE Select	ENSP00000490491.2:p.Glu1328Gln
ENST00000636940.1:n.1979G>C
ENST00000637015.1:c.1350G>C
ENST00000637568.1:c.1264G>C
ENST00000637741.1:n.648G>C
ENST00000637810.1:c.1324G>C	ENSP00000489636.1:p.Glu442Gln
ENST00000637904.1:c.1483G>C	ENSP00000490550.1:p.Glu495Gln
ENST00000647938.1:c.3613G>C	ENSP00000498155.1:p.Glu1205Gln
ENST00000346085.9:c.3613G>C	ENSP00000344546.4:p.Glu1205Gln
ENST00000350026.9:c.3574G>C	ENSP00000055163.7:p.Glu1192Gln
ENST00000414678.6:c.2140G>C	ENSP00000412835.2:p.Glu714Gln
NM_017519.2:c.3574G>C	NP_059989.2:p.Glu1192Gln
NM_020732.3:c.3613G>C	NP_065783.3:p.Glu1205Gln
XM_005267069.3:c.3733G>C	XP_005267126.2:p.Glu1245Gln
XM_011535984.1:c.2812G>C	XP_011534286.1:p.Glu938Gln
XM_011535985.1:c.2632G>C	XP_011534287.1:p.Glu878Gln
XM_011535986.1:c.2392G>C	XP_011534288.1:p.Glu798Gln
XM_011535987.1:c.2011G>C	XP_011534289.1:p.Glu671Gln
XM_011535988.1:c.874G>C	XP_011534290.1:p.Glu292Gln
NM_001346813.1:c.3733G>C	NP_001333742.1:p.Glu1245Gln
NM_001363725.1:c.1483G>C	NP_001350654.1:p.Glu495Gln
XM_011535984.2:c.3943G>C	XP_011534286.2:p.Glu1315Gln
XM_011535988.3:c.874G>C	XP_011534290.1:p.Glu292Gln
XM_017011103.2:c.3844G>C	XP_016866592.1:p.Glu1282Gln
XM_017011104.1:c.3814G>C	XP_016866593.1:p.Glu1272Gln
XM_017011105.2:c.3784G>C	XP_016866594.1:p.Glu1262Gln
XM_017011106.2:c.3655G>C	XP_016866595.1:p.Glu1219Gln
XM_017011107.2:c.3634G>C	XP_016866596.1:p.Glu1212Gln
XR_002956289.1:n.4026G>C
NM_001363725.2:c.1483G>C	NP_001350654.1:p.Glu495Gln
NM_001371656.1:c.3862G>C	NP_001358585.1:p.Glu1288Gln
NM_001374820.1:c.3862G>C	NP_001361749.1:p.Glu1288Gln
NM_001374828.1:c.3982G>C MANE Select	NP_001361757.1:p.Glu1328Gln
NM_017519.3:c.3823G>C	NP_059989.3:p.Glu1275Gln