Canonical Allele Identifier: CA366234264

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510893T>C (hg19) ; chr6:g.157189759T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189759T>C , CM000668.2:g.157189759T>C	GRCh38
NC_000006.11:g.157510893T>C , CM000668.1:g.157510893T>C	GRCh37
NC_000006.10:g.157552585T>C	NCBI36
NG_032093.1:g.416830T>C
NG_032093.2:g.416830T>C
NG_066624.1:g.418734T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3878T>C	ENSP00000055163.8:p.Met1293Thr
ENST00000414678.8:c.3947T>C	ENSP00000412835.3:p.Met1316Thr
ENST00000637015.2:c.4166T>C	ENSP00000489729.2:p.Met1389Thr
ENST00000346085.10:c.3917T>C	ENSP00000344546.5:p.Met1306Thr
ENST00000350026.10:c.3629T>C	ENSP00000055163.7:p.Met1210Thr
ENST00000414678.7:c.2195T>C	ENSP00000412835.2:p.Met732Thr
ENST00000635849.1:c.1358T>C	ENSP00000490948.1:p.Met453Thr
ENST00000635957.1:c.992T>C	ENSP00000490385.1:p.Met331Thr
ENST00000636930.2:c.4037T>C MANE Select	ENSP00000490491.2:p.Met1346Thr
ENST00000636940.1:n.2034T>C
ENST00000637015.1:c.1405T>C
ENST00000637568.1:c.1319T>C
ENST00000637741.1:n.703T>C
ENST00000637810.1:c.1379T>C	ENSP00000489636.1:p.Met460Thr
ENST00000637904.1:c.1538T>C	ENSP00000490550.1:p.Met513Thr
ENST00000647938.1:c.3668T>C	ENSP00000498155.1:p.Met1223Thr
ENST00000346085.9:c.3668T>C	ENSP00000344546.4:p.Met1223Thr
ENST00000350026.9:c.3629T>C	ENSP00000055163.7:p.Met1210Thr
ENST00000414678.6:c.2195T>C	ENSP00000412835.2:p.Met732Thr
NM_017519.2:c.3629T>C	NP_059989.2:p.Met1210Thr
NM_020732.3:c.3668T>C	NP_065783.3:p.Met1223Thr
XM_005267069.3:c.3788T>C	XP_005267126.2:p.Met1263Thr
XM_011535984.1:c.2867T>C	XP_011534286.1:p.Met956Thr
XM_011535985.1:c.2687T>C	XP_011534287.1:p.Met896Thr
XM_011535986.1:c.2447T>C	XP_011534288.1:p.Met816Thr
XM_011535987.1:c.2066T>C	XP_011534289.1:p.Met689Thr
XM_011535988.1:c.929T>C	XP_011534290.1:p.Met310Thr
NM_001346813.1:c.3788T>C	NP_001333742.1:p.Met1263Thr
NM_001363725.1:c.1538T>C	NP_001350654.1:p.Met513Thr
XM_011535984.2:c.3998T>C	XP_011534286.2:p.Met1333Thr
XM_011535988.3:c.929T>C	XP_011534290.1:p.Met310Thr
XM_017011103.2:c.3899T>C	XP_016866592.1:p.Met1300Thr
XM_017011104.1:c.3869T>C	XP_016866593.1:p.Met1290Thr
XM_017011105.2:c.3839T>C	XP_016866594.1:p.Met1280Thr
XM_017011106.2:c.3710T>C	XP_016866595.1:p.Met1237Thr
XM_017011107.2:c.3689T>C	XP_016866596.1:p.Met1230Thr
XR_002956289.1:n.4081T>C
NM_001363725.2:c.1538T>C	NP_001350654.1:p.Met513Thr
NM_001371656.1:c.3917T>C	NP_001358585.1:p.Met1306Thr
NM_001374820.1:c.3917T>C	NP_001361749.1:p.Met1306Thr
NM_001374828.1:c.4037T>C MANE Select	NP_001361757.1:p.Met1346Thr
NM_017519.3:c.3878T>C	NP_059989.3:p.Met1293Thr