Canonical Allele Identifier: CA366242323

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522379T>G (hg19) ; chr6:g.157201245T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201245T>G , CM000668.2:g.157201245T>G	GRCh38
NC_000006.11:g.157522379T>G , CM000668.1:g.157522379T>G	GRCh37
NC_000006.10:g.157564071T>G	NCBI36
NG_032093.1:g.428316T>G
NG_032093.2:g.428316T>G
NG_066624.1:g.430220T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4861T>G	ENSP00000055163.8:p.Ser1621Ala
ENST00000414678.8:c.4930T>G	ENSP00000412835.3:p.Ser1644Ala
ENST00000637015.2:c.5149T>G	ENSP00000489729.2:p.Ser1717Ala
ENST00000346085.10:c.4900T>G	ENSP00000344546.5:p.Ser1634Ala
ENST00000350026.10:c.4612T>G	ENSP00000055163.7:p.Ser1538Ala
ENST00000414678.7:c.3178T>G	ENSP00000412835.2:p.Ser1060Ala
ENST00000635849.1:c.2341T>G	ENSP00000490948.1:p.Ser781Ala
ENST00000635957.1:c.1972T>G	ENSP00000490385.1:p.Ser658Ala
ENST00000636227.1:n.3483T>G
ENST00000636254.1:n.940T>G
ENST00000636930.2:c.5020T>G MANE Select	ENSP00000490491.2:p.Ser1674Ala
ENST00000636940.1:n.3017T>G
ENST00000637015.1:c.2388T>G
ENST00000637568.1:c.2302T>G
ENST00000637741.1:n.1686T>G
ENST00000637810.1:c.2362T>G	ENSP00000489636.1:p.Ser788Ala
ENST00000637904.1:c.2521T>G	ENSP00000490550.1:p.Ser841Ala
ENST00000647938.1:c.4651T>G	ENSP00000498155.1:p.Ser1551Ala
ENST00000346085.9:c.4651T>G	ENSP00000344546.4:p.Ser1551Ala
ENST00000350026.9:c.4612T>G	ENSP00000055163.7:p.Ser1538Ala
ENST00000414678.6:c.3178T>G	ENSP00000412835.2:p.Ser1060Ala
NM_017519.2:c.4612T>G	NP_059989.2:p.Ser1538Ala
NM_020732.3:c.4651T>G	NP_065783.3:p.Ser1551Ala
XM_005267069.3:c.4771T>G	XP_005267126.2:p.Ser1591Ala
XM_011535984.1:c.3850T>G	XP_011534286.1:p.Ser1284Ala
XM_011535985.1:c.3670T>G	XP_011534287.1:p.Ser1224Ala
XM_011535986.1:c.3430T>G	XP_011534288.1:p.Ser1144Ala
XM_011535987.1:c.3049T>G	XP_011534289.1:p.Ser1017Ala
XM_011535988.1:c.1912T>G	XP_011534290.1:p.Ser638Ala
NM_001346813.1:c.4771T>G	NP_001333742.1:p.Ser1591Ala
NM_001363725.1:c.2521T>G	NP_001350654.1:p.Ser841Ala
XM_011535984.2:c.4981T>G	XP_011534286.2:p.Ser1661Ala
XM_011535988.3:c.1912T>G	XP_011534290.1:p.Ser638Ala
XM_017011103.2:c.4882T>G	XP_016866592.1:p.Ser1628Ala
XM_017011104.1:c.4852T>G	XP_016866593.1:p.Ser1618Ala
XM_017011105.2:c.4822T>G	XP_016866594.1:p.Ser1608Ala
XM_017011106.2:c.4693T>G	XP_016866595.1:p.Ser1565Ala
XM_017011107.2:c.4672T>G	XP_016866596.1:p.Ser1558Ala
XR_002956289.1:n.4967T>G
NM_001363725.2:c.2521T>G	NP_001350654.1:p.Ser841Ala
NM_001371656.1:c.4900T>G	NP_001358585.1:p.Ser1634Ala
NM_001374820.1:c.4900T>G	NP_001361749.1:p.Ser1634Ala
NM_001374828.1:c.5020T>G MANE Select	NP_001361757.1:p.Ser1674Ala
NM_017519.3:c.4861T>G	NP_059989.3:p.Ser1621Ala