Canonical Allele Identifier: CA366240917

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157521915A>C (hg19) ; chr6:g.157200781A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200781A>C , CM000668.2:g.157200781A>C	GRCh38
NC_000006.11:g.157521915A>C , CM000668.1:g.157521915A>C	GRCh37
NC_000006.10:g.157563607A>C	NCBI36
NG_032093.1:g.427852A>C
NG_032093.2:g.427852A>C
NG_066624.1:g.429756A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4397A>C	ENSP00000055163.8:p.Tyr1466Ser
ENST00000414678.8:c.4466A>C	ENSP00000412835.3:p.Tyr1489Ser
ENST00000637015.2:c.4685A>C	ENSP00000489729.2:p.Tyr1562Ser
ENST00000346085.10:c.4436A>C	ENSP00000344546.5:p.Tyr1479Ser
ENST00000350026.10:c.4148A>C	ENSP00000055163.7:p.Tyr1383Ser
ENST00000414678.7:c.2714A>C	ENSP00000412835.2:p.Tyr905Ser
ENST00000635849.1:c.1877A>C	ENSP00000490948.1:p.Tyr626Ser
ENST00000635957.1:c.1508A>C	ENSP00000490385.1:p.Tyr503Ser
ENST00000636227.1:n.3019A>C
ENST00000636254.1:n.476A>C
ENST00000636930.2:c.4556A>C MANE Select	ENSP00000490491.2:p.Tyr1519Ser
ENST00000636940.1:n.2553A>C
ENST00000637015.1:c.1924A>C
ENST00000637568.1:c.1838A>C
ENST00000637741.1:n.1222A>C
ENST00000637810.1:c.1898A>C	ENSP00000489636.1:p.Tyr633Ser
ENST00000637904.1:c.2057A>C	ENSP00000490550.1:p.Tyr686Ser
ENST00000647938.1:c.4187A>C	ENSP00000498155.1:p.Tyr1396Ser
ENST00000346085.9:c.4187A>C	ENSP00000344546.4:p.Tyr1396Ser
ENST00000350026.9:c.4148A>C	ENSP00000055163.7:p.Tyr1383Ser
ENST00000414678.6:c.2714A>C	ENSP00000412835.2:p.Tyr905Ser
NM_017519.2:c.4148A>C	NP_059989.2:p.Tyr1383Ser
NM_020732.3:c.4187A>C	NP_065783.3:p.Tyr1396Ser
XM_005267069.3:c.4307A>C	XP_005267126.2:p.Tyr1436Ser
XM_011535984.1:c.3386A>C	XP_011534286.1:p.Tyr1129Ser
XM_011535985.1:c.3206A>C	XP_011534287.1:p.Tyr1069Ser
XM_011535986.1:c.2966A>C	XP_011534288.1:p.Tyr989Ser
XM_011535987.1:c.2585A>C	XP_011534289.1:p.Tyr862Ser
XM_011535988.1:c.1448A>C	XP_011534290.1:p.Tyr483Ser
NM_001346813.1:c.4307A>C	NP_001333742.1:p.Tyr1436Ser
NM_001363725.1:c.2057A>C	NP_001350654.1:p.Tyr686Ser
XM_011535984.2:c.4517A>C	XP_011534286.2:p.Tyr1506Ser
XM_011535988.3:c.1448A>C	XP_011534290.1:p.Tyr483Ser
XM_017011103.2:c.4418A>C	XP_016866592.1:p.Tyr1473Ser
XM_017011104.1:c.4388A>C	XP_016866593.1:p.Tyr1463Ser
XM_017011105.2:c.4358A>C	XP_016866594.1:p.Tyr1453Ser
XM_017011106.2:c.4229A>C	XP_016866595.1:p.Tyr1410Ser
XM_017011107.2:c.4208A>C	XP_016866596.1:p.Tyr1403Ser
XR_002956289.1:n.4503A>C
NM_001363725.2:c.2057A>C	NP_001350654.1:p.Tyr686Ser
NM_001371656.1:c.4436A>C	NP_001358585.1:p.Tyr1479Ser
NM_001374820.1:c.4436A>C	NP_001361749.1:p.Tyr1479Ser
NM_001374828.1:c.4556A>C MANE Select	NP_001361757.1:p.Tyr1519Ser
NM_017519.3:c.4397A>C	NP_059989.3:p.Tyr1466Ser