Canonical Allele Identifier: CA366235330

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157511262C>G (hg19) ; chr6:g.157190128C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190128C>G , CM000668.2:g.157190128C>G	GRCh38
NC_000006.11:g.157511262C>G , CM000668.1:g.157511262C>G	GRCh37
NC_000006.10:g.157552954C>G	NCBI36
NG_032093.1:g.417199C>G
NG_032093.2:g.417199C>G
NG_066624.1:g.419103C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3990C>G	ENSP00000055163.8:p.Tyr1330Ter
ENST00000414678.8:c.4059C>G	ENSP00000412835.3:p.Tyr1353Ter
ENST00000637015.2:c.4278C>G	ENSP00000489729.2:p.Tyr1426Ter
ENST00000346085.10:c.4029C>G	ENSP00000344546.5:p.Tyr1343Ter
ENST00000350026.10:c.3741C>G	ENSP00000055163.7:p.Tyr1247Ter
ENST00000414678.7:c.2307C>G	ENSP00000412835.2:p.Tyr769Ter
ENST00000635849.1:c.1470C>G	ENSP00000490948.1:p.Tyr490Ter
ENST00000635957.1:c.1101C>G	ENSP00000490385.1:p.Tyr367Ter
ENST00000636930.2:c.4149C>G MANE Select	ENSP00000490491.2:p.Tyr1383Ter
ENST00000636940.1:n.2146C>G
ENST00000637015.1:c.1517C>G
ENST00000637568.1:c.1431C>G
ENST00000637741.1:n.815C>G
ENST00000637810.1:c.1491C>G	ENSP00000489636.1:p.Tyr497Ter
ENST00000637904.1:c.1650C>G	ENSP00000490550.1:p.Tyr550Ter
ENST00000647938.1:c.3780C>G	ENSP00000498155.1:p.Tyr1260Ter
ENST00000346085.9:c.3780C>G	ENSP00000344546.4:p.Tyr1260Ter
ENST00000350026.9:c.3741C>G	ENSP00000055163.7:p.Tyr1247Ter
ENST00000414678.6:c.2307C>G	ENSP00000412835.2:p.Tyr769Ter
NM_017519.2:c.3741C>G	NP_059989.2:p.Tyr1247Ter
NM_020732.3:c.3780C>G	NP_065783.3:p.Tyr1260Ter
XM_005267069.3:c.3900C>G	XP_005267126.2:p.Tyr1300Ter
XM_011535984.1:c.2979C>G	XP_011534286.1:p.Tyr993Ter
XM_011535985.1:c.2799C>G	XP_011534287.1:p.Tyr933Ter
XM_011535986.1:c.2559C>G	XP_011534288.1:p.Tyr853Ter
XM_011535987.1:c.2178C>G	XP_011534289.1:p.Tyr726Ter
XM_011535988.1:c.1041C>G	XP_011534290.1:p.Tyr347Ter
NM_001346813.1:c.3900C>G	NP_001333742.1:p.Tyr1300Ter
NM_001363725.1:c.1650C>G	NP_001350654.1:p.Tyr550Ter
XM_011535984.2:c.4110C>G	XP_011534286.2:p.Tyr1370Ter
XM_011535988.3:c.1041C>G	XP_011534290.1:p.Tyr347Ter
XM_017011103.2:c.4011C>G	XP_016866592.1:p.Tyr1337Ter
XM_017011104.1:c.3981C>G	XP_016866593.1:p.Tyr1327Ter
XM_017011105.2:c.3951C>G	XP_016866594.1:p.Tyr1317Ter
XM_017011106.2:c.3822C>G	XP_016866595.1:p.Tyr1274Ter
XM_017011107.2:c.3801C>G	XP_016866596.1:p.Tyr1267Ter
XR_002956289.1:n.4193C>G
NM_001363725.2:c.1650C>G	NP_001350654.1:p.Tyr550Ter
NM_001371656.1:c.4029C>G	NP_001358585.1:p.Tyr1343Ter
NM_001374820.1:c.4029C>G	NP_001361749.1:p.Tyr1343Ter
NM_001374828.1:c.4149C>G MANE Select	NP_001361757.1:p.Tyr1383Ter
NM_017519.3:c.3990C>G	NP_059989.3:p.Tyr1330Ter