Canonical Allele Identifier: CA366235297

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157511246C>G (hg19) ; chr6:g.157190112C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190112C>G , CM000668.2:g.157190112C>G	GRCh38
NC_000006.11:g.157511246C>G , CM000668.1:g.157511246C>G	GRCh37
NC_000006.10:g.157552938C>G	NCBI36
NG_032093.1:g.417183C>G
NG_032093.2:g.417183C>G
NG_066624.1:g.419087C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3974C>G	ENSP00000055163.8:p.Thr1325Ser
ENST00000414678.8:c.4043C>G	ENSP00000412835.3:p.Thr1348Ser
ENST00000637015.2:c.4262C>G	ENSP00000489729.2:p.Thr1421Ser
ENST00000346085.10:c.4013C>G	ENSP00000344546.5:p.Thr1338Ser
ENST00000350026.10:c.3725C>G	ENSP00000055163.7:p.Thr1242Ser
ENST00000414678.7:c.2291C>G	ENSP00000412835.2:p.Thr764Ser
ENST00000635849.1:c.1454C>G	ENSP00000490948.1:p.Thr485Ser
ENST00000635957.1:c.1085C>G	ENSP00000490385.1:p.Thr362Ser
ENST00000636930.2:c.4133C>G MANE Select	ENSP00000490491.2:p.Thr1378Ser
ENST00000636940.1:n.2130C>G
ENST00000637015.1:c.1501C>G
ENST00000637568.1:c.1415C>G
ENST00000637741.1:n.799C>G
ENST00000637810.1:c.1475C>G	ENSP00000489636.1:p.Thr492Ser
ENST00000637904.1:c.1634C>G	ENSP00000490550.1:p.Thr545Ser
ENST00000647938.1:c.3764C>G	ENSP00000498155.1:p.Thr1255Ser
ENST00000346085.9:c.3764C>G	ENSP00000344546.4:p.Thr1255Ser
ENST00000350026.9:c.3725C>G	ENSP00000055163.7:p.Thr1242Ser
ENST00000414678.6:c.2291C>G	ENSP00000412835.2:p.Thr764Ser
NM_017519.2:c.3725C>G	NP_059989.2:p.Thr1242Ser
NM_020732.3:c.3764C>G	NP_065783.3:p.Thr1255Ser
XM_005267069.3:c.3884C>G	XP_005267126.2:p.Thr1295Ser
XM_011535984.1:c.2963C>G	XP_011534286.1:p.Thr988Ser
XM_011535985.1:c.2783C>G	XP_011534287.1:p.Thr928Ser
XM_011535986.1:c.2543C>G	XP_011534288.1:p.Thr848Ser
XM_011535987.1:c.2162C>G	XP_011534289.1:p.Thr721Ser
XM_011535988.1:c.1025C>G	XP_011534290.1:p.Thr342Ser
NM_001346813.1:c.3884C>G	NP_001333742.1:p.Thr1295Ser
NM_001363725.1:c.1634C>G	NP_001350654.1:p.Thr545Ser
XM_011535984.2:c.4094C>G	XP_011534286.2:p.Thr1365Ser
XM_011535988.3:c.1025C>G	XP_011534290.1:p.Thr342Ser
XM_017011103.2:c.3995C>G	XP_016866592.1:p.Thr1332Ser
XM_017011104.1:c.3965C>G	XP_016866593.1:p.Thr1322Ser
XM_017011105.2:c.3935C>G	XP_016866594.1:p.Thr1312Ser
XM_017011106.2:c.3806C>G	XP_016866595.1:p.Thr1269Ser
XM_017011107.2:c.3785C>G	XP_016866596.1:p.Thr1262Ser
XR_002956289.1:n.4177C>G
NM_001363725.2:c.1634C>G	NP_001350654.1:p.Thr545Ser
NM_001371656.1:c.4013C>G	NP_001358585.1:p.Thr1338Ser
NM_001374820.1:c.4013C>G	NP_001361749.1:p.Thr1338Ser
NM_001374828.1:c.4133C>G MANE Select	NP_001361757.1:p.Thr1378Ser
NM_017519.3:c.3974C>G	NP_059989.3:p.Thr1325Ser