Canonical Allele Identifier: CA366228133

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157502251A>C (hg19) ; chr6:g.157181117A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181117A>C , CM000668.2:g.157181117A>C	GRCh38
NC_000006.11:g.157502251A>C , CM000668.1:g.157502251A>C	GRCh37
NC_000006.10:g.157543943A>C	NCBI36
NG_032093.1:g.408188A>C
NG_032093.2:g.408188A>C
NG_066624.1:g.410092A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3494A>C	ENSP00000055163.8:p.Lys1165Thr
ENST00000414678.8:c.3563A>C	ENSP00000412835.3:p.Lys1188Thr
ENST00000637015.2:c.3782A>C	ENSP00000489729.2:p.Lys1261Thr
ENST00000319584.11:c.1667A>C	ENSP00000313006.7:p.Lys556Thr
ENST00000346085.10:c.3533A>C	ENSP00000344546.5:p.Lys1178Thr
ENST00000350026.10:c.3245A>C	ENSP00000055163.7:p.Lys1082Thr
ENST00000414678.7:c.1811A>C	ENSP00000412835.2:p.Lys604Thr
ENST00000635849.1:c.974A>C	ENSP00000490948.1:p.Lys325Thr
ENST00000635957.1:c.608A>C	ENSP00000490385.1:p.Lys203Thr
ENST00000636930.2:c.3653A>C MANE Select	ENSP00000490491.2:p.Lys1218Thr
ENST00000636940.1:n.1650A>C
ENST00000637015.1:c.1021A>C
ENST00000637568.1:c.935A>C
ENST00000637741.1:n.319A>C
ENST00000637810.1:c.995A>C	ENSP00000489636.1:p.Lys332Thr
ENST00000637904.1:c.1154A>C	ENSP00000490550.1:p.Lys385Thr
ENST00000647938.1:c.3284A>C	ENSP00000498155.1:p.Lys1095Thr
ENST00000319584.10:c.1670A>C	ENSP00000313006.6:p.Lys557Thr
ENST00000346085.9:c.3284A>C	ENSP00000344546.4:p.Lys1095Thr
ENST00000350026.9:c.3245A>C	ENSP00000055163.7:p.Lys1082Thr
ENST00000400790.3:c.446A>C	ENSP00000383596.3:p.Lys149Thr
ENST00000414678.6:c.1811A>C	ENSP00000412835.2:p.Lys604Thr
ENST00000478761.3:c.855A>C
NM_017519.2:c.3245A>C	NP_059989.2:p.Lys1082Thr
NM_020732.3:c.3284A>C	NP_065783.3:p.Lys1095Thr
XM_005267069.3:c.3404A>C	XP_005267126.2:p.Lys1135Thr
XM_011535984.1:c.2483A>C	XP_011534286.1:p.Lys828Thr
XM_011535985.1:c.2303A>C	XP_011534287.1:p.Lys768Thr
XM_011535986.1:c.2063A>C	XP_011534288.1:p.Lys688Thr
XM_011535987.1:c.1682A>C	XP_011534289.1:p.Lys561Thr
XM_011535988.1:c.545A>C	XP_011534290.1:p.Lys182Thr
NM_001346813.1:c.3404A>C	NP_001333742.1:p.Lys1135Thr
NM_001363725.1:c.1154A>C	NP_001350654.1:p.Lys385Thr
XM_011535984.2:c.3614A>C	XP_011534286.2:p.Lys1205Thr
XM_011535988.3:c.545A>C	XP_011534290.1:p.Lys182Thr
XM_017011103.2:c.3515A>C	XP_016866592.1:p.Lys1172Thr
XM_017011104.1:c.3485A>C	XP_016866593.1:p.Lys1162Thr
XM_017011105.2:c.3455A>C	XP_016866594.1:p.Lys1152Thr
XM_017011106.2:c.3326A>C	XP_016866595.1:p.Lys1109Thr
XM_017011107.2:c.3305A>C	XP_016866596.1:p.Lys1102Thr
XR_002956289.1:n.3697A>C
NM_001363725.2:c.1154A>C	NP_001350654.1:p.Lys385Thr
NM_001371656.1:c.3533A>C	NP_001358585.1:p.Lys1178Thr
NM_001374820.1:c.3533A>C	NP_001361749.1:p.Lys1178Thr
NM_001374828.1:c.3653A>C MANE Select	NP_001361757.1:p.Lys1218Thr
NM_017519.3:c.3494A>C	NP_059989.3:p.Lys1165Thr