Canonical Allele Identifier: CA366234079

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510817A>T (hg19) ; chr6:g.157189683A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189683A>T , CM000668.2:g.157189683A>T	GRCh38
NC_000006.11:g.157510817A>T , CM000668.1:g.157510817A>T	GRCh37
NC_000006.10:g.157552509A>T	NCBI36
NG_032093.1:g.416754A>T
NG_032093.2:g.416754A>T
NG_066624.1:g.418658A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3802A>T	ENSP00000055163.8:p.Thr1268Ser
ENST00000414678.8:c.3871A>T	ENSP00000412835.3:p.Thr1291Ser
ENST00000637015.2:c.4090A>T	ENSP00000489729.2:p.Thr1364Ser
ENST00000346085.10:c.3841A>T	ENSP00000344546.5:p.Thr1281Ser
ENST00000350026.10:c.3553A>T	ENSP00000055163.7:p.Thr1185Ser
ENST00000414678.7:c.2119A>T	ENSP00000412835.2:p.Thr707Ser
ENST00000635849.1:c.1282A>T	ENSP00000490948.1:p.Thr428Ser
ENST00000635957.1:c.916A>T	ENSP00000490385.1:p.Thr306Ser
ENST00000636930.2:c.3961A>T MANE Select	ENSP00000490491.2:p.Thr1321Ser
ENST00000636940.1:n.1958A>T
ENST00000637015.1:c.1329A>T
ENST00000637568.1:c.1243A>T
ENST00000637741.1:n.627A>T
ENST00000637810.1:c.1303A>T	ENSP00000489636.1:p.Thr435Ser
ENST00000637904.1:c.1462A>T	ENSP00000490550.1:p.Thr488Ser
ENST00000647938.1:c.3592A>T	ENSP00000498155.1:p.Thr1198Ser
ENST00000346085.9:c.3592A>T	ENSP00000344546.4:p.Thr1198Ser
ENST00000350026.9:c.3553A>T	ENSP00000055163.7:p.Thr1185Ser
ENST00000414678.6:c.2119A>T	ENSP00000412835.2:p.Thr707Ser
NM_017519.2:c.3553A>T	NP_059989.2:p.Thr1185Ser
NM_020732.3:c.3592A>T	NP_065783.3:p.Thr1198Ser
XM_005267069.3:c.3712A>T	XP_005267126.2:p.Thr1238Ser
XM_011535984.1:c.2791A>T	XP_011534286.1:p.Thr931Ser
XM_011535985.1:c.2611A>T	XP_011534287.1:p.Thr871Ser
XM_011535986.1:c.2371A>T	XP_011534288.1:p.Thr791Ser
XM_011535987.1:c.1990A>T	XP_011534289.1:p.Thr664Ser
XM_011535988.1:c.853A>T	XP_011534290.1:p.Thr285Ser
NM_001346813.1:c.3712A>T	NP_001333742.1:p.Thr1238Ser
NM_001363725.1:c.1462A>T	NP_001350654.1:p.Thr488Ser
XM_011535984.2:c.3922A>T	XP_011534286.2:p.Thr1308Ser
XM_011535988.3:c.853A>T	XP_011534290.1:p.Thr285Ser
XM_017011103.2:c.3823A>T	XP_016866592.1:p.Thr1275Ser
XM_017011104.1:c.3793A>T	XP_016866593.1:p.Thr1265Ser
XM_017011105.2:c.3763A>T	XP_016866594.1:p.Thr1255Ser
XM_017011106.2:c.3634A>T	XP_016866595.1:p.Thr1212Ser
XM_017011107.2:c.3613A>T	XP_016866596.1:p.Thr1205Ser
XR_002956289.1:n.4005A>T
NM_001363725.2:c.1462A>T	NP_001350654.1:p.Thr488Ser
NM_001371656.1:c.3841A>T	NP_001358585.1:p.Thr1281Ser
NM_001374820.1:c.3841A>T	NP_001361749.1:p.Thr1281Ser
NM_001374828.1:c.3961A>T MANE Select	NP_001361757.1:p.Thr1321Ser
NM_017519.3:c.3802A>T	NP_059989.3:p.Thr1268Ser