Canonical Allele Identifier: CA366234072

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510814T>A (hg19) ; chr6:g.157189680T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189680T>A , CM000668.2:g.157189680T>A	GRCh38
NC_000006.11:g.157510814T>A , CM000668.1:g.157510814T>A	GRCh37
NC_000006.10:g.157552506T>A	NCBI36
NG_032093.1:g.416751T>A
NG_032093.2:g.416751T>A
NG_066624.1:g.418655T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3799T>A	ENSP00000055163.8:p.Ser1267Thr
ENST00000414678.8:c.3868T>A	ENSP00000412835.3:p.Ser1290Thr
ENST00000637015.2:c.4087T>A	ENSP00000489729.2:p.Ser1363Thr
ENST00000346085.10:c.3838T>A	ENSP00000344546.5:p.Ser1280Thr
ENST00000350026.10:c.3550T>A	ENSP00000055163.7:p.Ser1184Thr
ENST00000414678.7:c.2116T>A	ENSP00000412835.2:p.Ser706Thr
ENST00000635849.1:c.1279T>A	ENSP00000490948.1:p.Ser427Thr
ENST00000635957.1:c.913T>A	ENSP00000490385.1:p.Ser305Thr
ENST00000636930.2:c.3958T>A MANE Select	ENSP00000490491.2:p.Ser1320Thr
ENST00000636940.1:n.1955T>A
ENST00000637015.1:c.1326T>A
ENST00000637568.1:c.1240T>A
ENST00000637741.1:n.624T>A
ENST00000637810.1:c.1300T>A	ENSP00000489636.1:p.Ser434Thr
ENST00000637904.1:c.1459T>A	ENSP00000490550.1:p.Ser487Thr
ENST00000647938.1:c.3589T>A	ENSP00000498155.1:p.Ser1197Thr
ENST00000346085.9:c.3589T>A	ENSP00000344546.4:p.Ser1197Thr
ENST00000350026.9:c.3550T>A	ENSP00000055163.7:p.Ser1184Thr
ENST00000414678.6:c.2116T>A	ENSP00000412835.2:p.Ser706Thr
NM_017519.2:c.3550T>A	NP_059989.2:p.Ser1184Thr
NM_020732.3:c.3589T>A	NP_065783.3:p.Ser1197Thr
XM_005267069.3:c.3709T>A	XP_005267126.2:p.Ser1237Thr
XM_011535984.1:c.2788T>A	XP_011534286.1:p.Ser930Thr
XM_011535985.1:c.2608T>A	XP_011534287.1:p.Ser870Thr
XM_011535986.1:c.2368T>A	XP_011534288.1:p.Ser790Thr
XM_011535987.1:c.1987T>A	XP_011534289.1:p.Ser663Thr
XM_011535988.1:c.850T>A	XP_011534290.1:p.Ser284Thr
NM_001346813.1:c.3709T>A	NP_001333742.1:p.Ser1237Thr
NM_001363725.1:c.1459T>A	NP_001350654.1:p.Ser487Thr
XM_011535984.2:c.3919T>A	XP_011534286.2:p.Ser1307Thr
XM_011535988.3:c.850T>A	XP_011534290.1:p.Ser284Thr
XM_017011103.2:c.3820T>A	XP_016866592.1:p.Ser1274Thr
XM_017011104.1:c.3790T>A	XP_016866593.1:p.Ser1264Thr
XM_017011105.2:c.3760T>A	XP_016866594.1:p.Ser1254Thr
XM_017011106.2:c.3631T>A	XP_016866595.1:p.Ser1211Thr
XM_017011107.2:c.3610T>A	XP_016866596.1:p.Ser1204Thr
XR_002956289.1:n.4002T>A
NM_001363725.2:c.1459T>A	NP_001350654.1:p.Ser487Thr
NM_001371656.1:c.3838T>A	NP_001358585.1:p.Ser1280Thr
NM_001374820.1:c.3838T>A	NP_001361749.1:p.Ser1280Thr
NM_001374828.1:c.3958T>A MANE Select	NP_001361757.1:p.Ser1320Thr
NM_017519.3:c.3799T>A	NP_059989.3:p.Ser1267Thr