Canonical Allele Identifier: CA366234199

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510875C>A (hg19) ; chr6:g.157189741C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189741C>A , CM000668.2:g.157189741C>A	GRCh38
NC_000006.11:g.157510875C>A , CM000668.1:g.157510875C>A	GRCh37
NC_000006.10:g.157552567C>A	NCBI36
NG_032093.1:g.416812C>A
NG_032093.2:g.416812C>A
NG_066624.1:g.418716C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3860C>A	ENSP00000055163.8:p.Ser1287Tyr
ENST00000414678.8:c.3929C>A	ENSP00000412835.3:p.Ser1310Tyr
ENST00000637015.2:c.4148C>A	ENSP00000489729.2:p.Ser1383Tyr
ENST00000346085.10:c.3899C>A	ENSP00000344546.5:p.Ser1300Tyr
ENST00000350026.10:c.3611C>A	ENSP00000055163.7:p.Ser1204Tyr
ENST00000414678.7:c.2177C>A	ENSP00000412835.2:p.Ser726Tyr
ENST00000635849.1:c.1340C>A	ENSP00000490948.1:p.Ser447Tyr
ENST00000635957.1:c.974C>A	ENSP00000490385.1:p.Ser325Tyr
ENST00000636930.2:c.4019C>A MANE Select	ENSP00000490491.2:p.Ser1340Tyr
ENST00000636940.1:n.2016C>A
ENST00000637015.1:c.1387C>A
ENST00000637568.1:c.1301C>A
ENST00000637741.1:n.685C>A
ENST00000637810.1:c.1361C>A	ENSP00000489636.1:p.Ser454Tyr
ENST00000637904.1:c.1520C>A	ENSP00000490550.1:p.Ser507Tyr
ENST00000647938.1:c.3650C>A	ENSP00000498155.1:p.Ser1217Tyr
ENST00000346085.9:c.3650C>A	ENSP00000344546.4:p.Ser1217Tyr
ENST00000350026.9:c.3611C>A	ENSP00000055163.7:p.Ser1204Tyr
ENST00000414678.6:c.2177C>A	ENSP00000412835.2:p.Ser726Tyr
NM_017519.2:c.3611C>A	NP_059989.2:p.Ser1204Tyr
NM_020732.3:c.3650C>A	NP_065783.3:p.Ser1217Tyr
XM_005267069.3:c.3770C>A	XP_005267126.2:p.Ser1257Tyr
XM_011535984.1:c.2849C>A	XP_011534286.1:p.Ser950Tyr
XM_011535985.1:c.2669C>A	XP_011534287.1:p.Ser890Tyr
XM_011535986.1:c.2429C>A	XP_011534288.1:p.Ser810Tyr
XM_011535987.1:c.2048C>A	XP_011534289.1:p.Ser683Tyr
XM_011535988.1:c.911C>A	XP_011534290.1:p.Ser304Tyr
NM_001346813.1:c.3770C>A	NP_001333742.1:p.Ser1257Tyr
NM_001363725.1:c.1520C>A	NP_001350654.1:p.Ser507Tyr
XM_011535984.2:c.3980C>A	XP_011534286.2:p.Ser1327Tyr
XM_011535988.3:c.911C>A	XP_011534290.1:p.Ser304Tyr
XM_017011103.2:c.3881C>A	XP_016866592.1:p.Ser1294Tyr
XM_017011104.1:c.3851C>A	XP_016866593.1:p.Ser1284Tyr
XM_017011105.2:c.3821C>A	XP_016866594.1:p.Ser1274Tyr
XM_017011106.2:c.3692C>A	XP_016866595.1:p.Ser1231Tyr
XM_017011107.2:c.3671C>A	XP_016866596.1:p.Ser1224Tyr
XR_002956289.1:n.4063C>A
NM_001363725.2:c.1520C>A	NP_001350654.1:p.Ser507Tyr
NM_001371656.1:c.3899C>A	NP_001358585.1:p.Ser1300Tyr
NM_001374820.1:c.3899C>A	NP_001361749.1:p.Ser1300Tyr
NM_001374828.1:c.4019C>A MANE Select	NP_001361757.1:p.Ser1340Tyr
NM_017519.3:c.3860C>A	NP_059989.3:p.Ser1287Tyr