Canonical Allele Identifier: CA366242268

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522352A>T (hg19) ; chr6:g.157201218A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201218A>T , CM000668.2:g.157201218A>T	GRCh38
NC_000006.11:g.157522352A>T , CM000668.1:g.157522352A>T	GRCh37
NC_000006.10:g.157564044A>T	NCBI36
NG_032093.1:g.428289A>T
NG_032093.2:g.428289A>T
NG_066624.1:g.430193A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4834A>T	ENSP00000055163.8:p.Thr1612Ser
ENST00000414678.8:c.4903A>T	ENSP00000412835.3:p.Thr1635Ser
ENST00000637015.2:c.5122A>T	ENSP00000489729.2:p.Thr1708Ser
ENST00000346085.10:c.4873A>T	ENSP00000344546.5:p.Thr1625Ser
ENST00000350026.10:c.4585A>T	ENSP00000055163.7:p.Thr1529Ser
ENST00000414678.7:c.3151A>T	ENSP00000412835.2:p.Thr1051Ser
ENST00000635849.1:c.2314A>T	ENSP00000490948.1:p.Thr772Ser
ENST00000635957.1:c.1945A>T	ENSP00000490385.1:p.Thr649Ser
ENST00000636227.1:n.3456A>T
ENST00000636254.1:n.913A>T
ENST00000636930.2:c.4993A>T MANE Select	ENSP00000490491.2:p.Thr1665Ser
ENST00000636940.1:n.2990A>T
ENST00000637015.1:c.2361A>T
ENST00000637568.1:c.2275A>T
ENST00000637741.1:n.1659A>T
ENST00000637810.1:c.2335A>T	ENSP00000489636.1:p.Thr779Ser
ENST00000637904.1:c.2494A>T	ENSP00000490550.1:p.Thr832Ser
ENST00000647938.1:c.4624A>T	ENSP00000498155.1:p.Thr1542Ser
ENST00000346085.9:c.4624A>T	ENSP00000344546.4:p.Thr1542Ser
ENST00000350026.9:c.4585A>T	ENSP00000055163.7:p.Thr1529Ser
ENST00000414678.6:c.3151A>T	ENSP00000412835.2:p.Thr1051Ser
NM_017519.2:c.4585A>T	NP_059989.2:p.Thr1529Ser
NM_020732.3:c.4624A>T	NP_065783.3:p.Thr1542Ser
XM_005267069.3:c.4744A>T	XP_005267126.2:p.Thr1582Ser
XM_011535984.1:c.3823A>T	XP_011534286.1:p.Thr1275Ser
XM_011535985.1:c.3643A>T	XP_011534287.1:p.Thr1215Ser
XM_011535986.1:c.3403A>T	XP_011534288.1:p.Thr1135Ser
XM_011535987.1:c.3022A>T	XP_011534289.1:p.Thr1008Ser
XM_011535988.1:c.1885A>T	XP_011534290.1:p.Thr629Ser
NM_001346813.1:c.4744A>T	NP_001333742.1:p.Thr1582Ser
NM_001363725.1:c.2494A>T	NP_001350654.1:p.Thr832Ser
XM_011535984.2:c.4954A>T	XP_011534286.2:p.Thr1652Ser
XM_011535988.3:c.1885A>T	XP_011534290.1:p.Thr629Ser
XM_017011103.2:c.4855A>T	XP_016866592.1:p.Thr1619Ser
XM_017011104.1:c.4825A>T	XP_016866593.1:p.Thr1609Ser
XM_017011105.2:c.4795A>T	XP_016866594.1:p.Thr1599Ser
XM_017011106.2:c.4666A>T	XP_016866595.1:p.Thr1556Ser
XM_017011107.2:c.4645A>T	XP_016866596.1:p.Thr1549Ser
XR_002956289.1:n.4940A>T
NM_001363725.2:c.2494A>T	NP_001350654.1:p.Thr832Ser
NM_001371656.1:c.4873A>T	NP_001358585.1:p.Thr1625Ser
NM_001374820.1:c.4873A>T	NP_001361749.1:p.Thr1625Ser
NM_001374828.1:c.4993A>T MANE Select	NP_001361757.1:p.Thr1665Ser
NM_017519.3:c.4834A>T	NP_059989.3:p.Thr1612Ser