Canonical Allele Identifier: CA366234650

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157511178T>G (hg19) ; chr6:g.157190044T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190044T>G , CM000668.2:g.157190044T>G	GRCh38
NC_000006.11:g.157511178T>G , CM000668.1:g.157511178T>G	GRCh37
NC_000006.10:g.157552870T>G	NCBI36
NG_032093.1:g.417115T>G
NG_032093.2:g.417115T>G
NG_066624.1:g.419019T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3906T>G	ENSP00000055163.8:p.Ser1302Arg
ENST00000414678.8:c.3975T>G	ENSP00000412835.3:p.Ser1325Arg
ENST00000637015.2:c.4194T>G	ENSP00000489729.2:p.Ser1398Arg
ENST00000346085.10:c.3945T>G	ENSP00000344546.5:p.Ser1315Arg
ENST00000350026.10:c.3657T>G	ENSP00000055163.7:p.Ser1219Arg
ENST00000414678.7:c.2223T>G	ENSP00000412835.2:p.Ser741Arg
ENST00000635849.1:c.1386T>G	ENSP00000490948.1:p.Ser462Arg
ENST00000635957.1:c.1017T>G	ENSP00000490385.1:p.Ser339Arg
ENST00000636930.2:c.4065T>G MANE Select	ENSP00000490491.2:p.Ser1355Arg
ENST00000636940.1:n.2062T>G
ENST00000637015.1:c.1433T>G
ENST00000637568.1:c.1347T>G
ENST00000637741.1:n.731T>G
ENST00000637810.1:c.1407T>G	ENSP00000489636.1:p.Ser469Arg
ENST00000637904.1:c.1566T>G	ENSP00000490550.1:p.Ser522Arg
ENST00000647938.1:c.3696T>G	ENSP00000498155.1:p.Ser1232Arg
ENST00000346085.9:c.3696T>G	ENSP00000344546.4:p.Ser1232Arg
ENST00000350026.9:c.3657T>G	ENSP00000055163.7:p.Ser1219Arg
ENST00000414678.6:c.2223T>G	ENSP00000412835.2:p.Ser741Arg
NM_017519.2:c.3657T>G	NP_059989.2:p.Ser1219Arg
NM_020732.3:c.3696T>G	NP_065783.3:p.Ser1232Arg
XM_005267069.3:c.3816T>G	XP_005267126.2:p.Ser1272Arg
XM_011535984.1:c.2895T>G	XP_011534286.1:p.Ser965Arg
XM_011535985.1:c.2715T>G	XP_011534287.1:p.Ser905Arg
XM_011535986.1:c.2475T>G	XP_011534288.1:p.Ser825Arg
XM_011535987.1:c.2094T>G	XP_011534289.1:p.Ser698Arg
XM_011535988.1:c.957T>G	XP_011534290.1:p.Ser319Arg
NM_001346813.1:c.3816T>G	NP_001333742.1:p.Ser1272Arg
NM_001363725.1:c.1566T>G	NP_001350654.1:p.Ser522Arg
XM_011535984.2:c.4026T>G	XP_011534286.2:p.Ser1342Arg
XM_011535988.3:c.957T>G	XP_011534290.1:p.Ser319Arg
XM_017011103.2:c.3927T>G	XP_016866592.1:p.Ser1309Arg
XM_017011104.1:c.3897T>G	XP_016866593.1:p.Ser1299Arg
XM_017011105.2:c.3867T>G	XP_016866594.1:p.Ser1289Arg
XM_017011106.2:c.3738T>G	XP_016866595.1:p.Ser1246Arg
XM_017011107.2:c.3717T>G	XP_016866596.1:p.Ser1239Arg
XR_002956289.1:n.4109T>G
NM_001363725.2:c.1566T>G	NP_001350654.1:p.Ser522Arg
NM_001371656.1:c.3945T>G	NP_001358585.1:p.Ser1315Arg
NM_001374820.1:c.3945T>G	NP_001361749.1:p.Ser1315Arg
NM_001374828.1:c.4065T>G MANE Select	NP_001361757.1:p.Ser1355Arg
NM_017519.3:c.3906T>G	NP_059989.3:p.Ser1302Arg