Canonical Allele Identifier: CA366242252

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522346T>G (hg19) ; chr6:g.157201212T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201212T>G , CM000668.2:g.157201212T>G	GRCh38
NC_000006.11:g.157522346T>G , CM000668.1:g.157522346T>G	GRCh37
NC_000006.10:g.157564038T>G	NCBI36
NG_032093.1:g.428283T>G
NG_032093.2:g.428283T>G
NG_066624.1:g.430187T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4828T>G	ENSP00000055163.8:p.Tyr1610Asp
ENST00000414678.8:c.4897T>G	ENSP00000412835.3:p.Tyr1633Asp
ENST00000637015.2:c.5116T>G	ENSP00000489729.2:p.Tyr1706Asp
ENST00000346085.10:c.4867T>G	ENSP00000344546.5:p.Tyr1623Asp
ENST00000350026.10:c.4579T>G	ENSP00000055163.7:p.Tyr1527Asp
ENST00000414678.7:c.3145T>G	ENSP00000412835.2:p.Tyr1049Asp
ENST00000635849.1:c.2308T>G	ENSP00000490948.1:p.Tyr770Asp
ENST00000635957.1:c.1939T>G	ENSP00000490385.1:p.Tyr647Asp
ENST00000636227.1:n.3450T>G
ENST00000636254.1:n.907T>G
ENST00000636930.2:c.4987T>G MANE Select	ENSP00000490491.2:p.Tyr1663Asp
ENST00000636940.1:n.2984T>G
ENST00000637015.1:c.2355T>G
ENST00000637568.1:c.2269T>G
ENST00000637741.1:n.1653T>G
ENST00000637810.1:c.2329T>G	ENSP00000489636.1:p.Tyr777Asp
ENST00000637904.1:c.2488T>G	ENSP00000490550.1:p.Tyr830Asp
ENST00000647938.1:c.4618T>G	ENSP00000498155.1:p.Tyr1540Asp
ENST00000346085.9:c.4618T>G	ENSP00000344546.4:p.Tyr1540Asp
ENST00000350026.9:c.4579T>G	ENSP00000055163.7:p.Tyr1527Asp
ENST00000414678.6:c.3145T>G	ENSP00000412835.2:p.Tyr1049Asp
NM_017519.2:c.4579T>G	NP_059989.2:p.Tyr1527Asp
NM_020732.3:c.4618T>G	NP_065783.3:p.Tyr1540Asp
XM_005267069.3:c.4738T>G	XP_005267126.2:p.Tyr1580Asp
XM_011535984.1:c.3817T>G	XP_011534286.1:p.Tyr1273Asp
XM_011535985.1:c.3637T>G	XP_011534287.1:p.Tyr1213Asp
XM_011535986.1:c.3397T>G	XP_011534288.1:p.Tyr1133Asp
XM_011535987.1:c.3016T>G	XP_011534289.1:p.Tyr1006Asp
XM_011535988.1:c.1879T>G	XP_011534290.1:p.Tyr627Asp
NM_001346813.1:c.4738T>G	NP_001333742.1:p.Tyr1580Asp
NM_001363725.1:c.2488T>G	NP_001350654.1:p.Tyr830Asp
XM_011535984.2:c.4948T>G	XP_011534286.2:p.Tyr1650Asp
XM_011535988.3:c.1879T>G	XP_011534290.1:p.Tyr627Asp
XM_017011103.2:c.4849T>G	XP_016866592.1:p.Tyr1617Asp
XM_017011104.1:c.4819T>G	XP_016866593.1:p.Tyr1607Asp
XM_017011105.2:c.4789T>G	XP_016866594.1:p.Tyr1597Asp
XM_017011106.2:c.4660T>G	XP_016866595.1:p.Tyr1554Asp
XM_017011107.2:c.4639T>G	XP_016866596.1:p.Tyr1547Asp
XR_002956289.1:n.4934T>G
NM_001363725.2:c.2488T>G	NP_001350654.1:p.Tyr830Asp
NM_001371656.1:c.4867T>G	NP_001358585.1:p.Tyr1623Asp
NM_001374820.1:c.4867T>G	NP_001361749.1:p.Tyr1623Asp
NM_001374828.1:c.4987T>G MANE Select	NP_001361757.1:p.Tyr1663Asp
NM_017519.3:c.4828T>G	NP_059989.3:p.Tyr1610Asp