Canonical Allele Identifier: CA366241376

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522121T>G (hg19) ; chr6:g.157200987T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200987T>G , CM000668.2:g.157200987T>G	GRCh38
NC_000006.11:g.157522121T>G , CM000668.1:g.157522121T>G	GRCh37
NC_000006.10:g.157563813T>G	NCBI36
NG_032093.1:g.428058T>G
NG_032093.2:g.428058T>G
NG_066624.1:g.429962T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4603T>G	ENSP00000055163.8:p.Trp1535Gly
ENST00000414678.8:c.4672T>G	ENSP00000412835.3:p.Trp1558Gly
ENST00000637015.2:c.4891T>G	ENSP00000489729.2:p.Trp1631Gly
ENST00000346085.10:c.4642T>G	ENSP00000344546.5:p.Trp1548Gly
ENST00000350026.10:c.4354T>G	ENSP00000055163.7:p.Trp1452Gly
ENST00000414678.7:c.2920T>G	ENSP00000412835.2:p.Trp974Gly
ENST00000635849.1:c.2083T>G	ENSP00000490948.1:p.Trp695Gly
ENST00000635957.1:c.1714T>G	ENSP00000490385.1:p.Trp572Gly
ENST00000636227.1:n.3225T>G
ENST00000636254.1:n.682T>G
ENST00000636930.2:c.4762T>G MANE Select	ENSP00000490491.2:p.Trp1588Gly
ENST00000636940.1:n.2759T>G
ENST00000637015.1:c.2130T>G
ENST00000637568.1:c.2044T>G
ENST00000637741.1:n.1428T>G
ENST00000637810.1:c.2104T>G	ENSP00000489636.1:p.Trp702Gly
ENST00000637904.1:c.2263T>G	ENSP00000490550.1:p.Trp755Gly
ENST00000647938.1:c.4393T>G	ENSP00000498155.1:p.Trp1465Gly
ENST00000346085.9:c.4393T>G	ENSP00000344546.4:p.Trp1465Gly
ENST00000350026.9:c.4354T>G	ENSP00000055163.7:p.Trp1452Gly
ENST00000414678.6:c.2920T>G	ENSP00000412835.2:p.Trp974Gly
NM_017519.2:c.4354T>G	NP_059989.2:p.Trp1452Gly
NM_020732.3:c.4393T>G	NP_065783.3:p.Trp1465Gly
XM_005267069.3:c.4513T>G	XP_005267126.2:p.Trp1505Gly
XM_011535984.1:c.3592T>G	XP_011534286.1:p.Trp1198Gly
XM_011535985.1:c.3412T>G	XP_011534287.1:p.Trp1138Gly
XM_011535986.1:c.3172T>G	XP_011534288.1:p.Trp1058Gly
XM_011535987.1:c.2791T>G	XP_011534289.1:p.Trp931Gly
XM_011535988.1:c.1654T>G	XP_011534290.1:p.Trp552Gly
NM_001346813.1:c.4513T>G	NP_001333742.1:p.Trp1505Gly
NM_001363725.1:c.2263T>G	NP_001350654.1:p.Trp755Gly
XM_011535984.2:c.4723T>G	XP_011534286.2:p.Trp1575Gly
XM_011535988.3:c.1654T>G	XP_011534290.1:p.Trp552Gly
XM_017011103.2:c.4624T>G	XP_016866592.1:p.Trp1542Gly
XM_017011104.1:c.4594T>G	XP_016866593.1:p.Trp1532Gly
XM_017011105.2:c.4564T>G	XP_016866594.1:p.Trp1522Gly
XM_017011106.2:c.4435T>G	XP_016866595.1:p.Trp1479Gly
XM_017011107.2:c.4414T>G	XP_016866596.1:p.Trp1472Gly
XR_002956289.1:n.4709T>G
NM_001363725.2:c.2263T>G	NP_001350654.1:p.Trp755Gly
NM_001371656.1:c.4642T>G	NP_001358585.1:p.Trp1548Gly
NM_001374820.1:c.4642T>G	NP_001361749.1:p.Trp1548Gly
NM_001374828.1:c.4762T>G MANE Select	NP_001361757.1:p.Trp1588Gly
NM_017519.3:c.4603T>G	NP_059989.3:p.Trp1535Gly