Canonical Allele Identifier: CA366234002

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510781T>A (hg19) ; chr6:g.157189647T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189647T>A , CM000668.2:g.157189647T>A	GRCh38
NC_000006.11:g.157510781T>A , CM000668.1:g.157510781T>A	GRCh37
NC_000006.10:g.157552473T>A	NCBI36
NG_032093.1:g.416718T>A
NG_032093.2:g.416718T>A
NG_066624.1:g.418622T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3766T>A	ENSP00000055163.8:p.Ser1256Thr
ENST00000414678.8:c.3835T>A	ENSP00000412835.3:p.Ser1279Thr
ENST00000637015.2:c.4054T>A	ENSP00000489729.2:p.Ser1352Thr
ENST00000346085.10:c.3805T>A	ENSP00000344546.5:p.Ser1269Thr
ENST00000350026.10:c.3517T>A	ENSP00000055163.7:p.Ser1173Thr
ENST00000414678.7:c.2083T>A	ENSP00000412835.2:p.Ser695Thr
ENST00000635849.1:c.1246T>A	ENSP00000490948.1:p.Ser416Thr
ENST00000635957.1:c.880T>A	ENSP00000490385.1:p.Ser294Thr
ENST00000636930.2:c.3925T>A MANE Select	ENSP00000490491.2:p.Ser1309Thr
ENST00000636940.1:n.1922T>A
ENST00000637015.1:c.1293T>A
ENST00000637568.1:c.1207T>A
ENST00000637741.1:n.591T>A
ENST00000637810.1:c.1267T>A	ENSP00000489636.1:p.Ser423Thr
ENST00000637904.1:c.1426T>A	ENSP00000490550.1:p.Ser476Thr
ENST00000647938.1:c.3556T>A	ENSP00000498155.1:p.Ser1186Thr
ENST00000346085.9:c.3556T>A	ENSP00000344546.4:p.Ser1186Thr
ENST00000350026.9:c.3517T>A	ENSP00000055163.7:p.Ser1173Thr
ENST00000414678.6:c.2083T>A	ENSP00000412835.2:p.Ser695Thr
NM_017519.2:c.3517T>A	NP_059989.2:p.Ser1173Thr
NM_020732.3:c.3556T>A	NP_065783.3:p.Ser1186Thr
XM_005267069.3:c.3676T>A	XP_005267126.2:p.Ser1226Thr
XM_011535984.1:c.2755T>A	XP_011534286.1:p.Ser919Thr
XM_011535985.1:c.2575T>A	XP_011534287.1:p.Ser859Thr
XM_011535986.1:c.2335T>A	XP_011534288.1:p.Ser779Thr
XM_011535987.1:c.1954T>A	XP_011534289.1:p.Ser652Thr
XM_011535988.1:c.817T>A	XP_011534290.1:p.Ser273Thr
NM_001346813.1:c.3676T>A	NP_001333742.1:p.Ser1226Thr
NM_001363725.1:c.1426T>A	NP_001350654.1:p.Ser476Thr
XM_011535984.2:c.3886T>A	XP_011534286.2:p.Ser1296Thr
XM_011535988.3:c.817T>A	XP_011534290.1:p.Ser273Thr
XM_017011103.2:c.3787T>A	XP_016866592.1:p.Ser1263Thr
XM_017011104.1:c.3757T>A	XP_016866593.1:p.Ser1253Thr
XM_017011105.2:c.3727T>A	XP_016866594.1:p.Ser1243Thr
XM_017011106.2:c.3598T>A	XP_016866595.1:p.Ser1200Thr
XM_017011107.2:c.3577T>A	XP_016866596.1:p.Ser1193Thr
XR_002956289.1:n.3969T>A
NM_001363725.2:c.1426T>A	NP_001350654.1:p.Ser476Thr
NM_001371656.1:c.3805T>A	NP_001358585.1:p.Ser1269Thr
NM_001374820.1:c.3805T>A	NP_001361749.1:p.Ser1269Thr
NM_001374828.1:c.3925T>A MANE Select	NP_001361757.1:p.Ser1309Thr
NM_017519.3:c.3766T>A	NP_059989.3:p.Ser1256Thr