Canonical Allele Identifier: CA366242746

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522496T>G (hg19) ; chr6:g.157201362T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201362T>G , CM000668.2:g.157201362T>G	GRCh38
NC_000006.11:g.157522496T>G , CM000668.1:g.157522496T>G	GRCh37
NC_000006.10:g.157564188T>G	NCBI36
NG_032093.1:g.428433T>G
NG_032093.2:g.428433T>G
NG_066624.1:g.430337T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4978T>G	ENSP00000055163.8:p.Ser1660Ala
ENST00000414678.8:c.5047T>G	ENSP00000412835.3:p.Ser1683Ala
ENST00000637015.2:c.5266T>G	ENSP00000489729.2:p.Ser1756Ala
ENST00000346085.10:c.5017T>G	ENSP00000344546.5:p.Ser1673Ala
ENST00000350026.10:c.4729T>G	ENSP00000055163.7:p.Ser1577Ala
ENST00000414678.7:c.3295T>G	ENSP00000412835.2:p.Ser1099Ala
ENST00000635849.1:c.2458T>G	ENSP00000490948.1:p.Ser820Ala
ENST00000635957.1:c.2089T>G	ENSP00000490385.1:p.Ser697Ala
ENST00000636227.1:n.3600T>G
ENST00000636254.1:n.1057T>G
ENST00000636930.2:c.5137T>G MANE Select	ENSP00000490491.2:p.Ser1713Ala
ENST00000636940.1:n.3134T>G
ENST00000637015.1:c.2505T>G
ENST00000637568.1:c.2419T>G
ENST00000637741.1:n.1803T>G
ENST00000637810.1:c.2479T>G	ENSP00000489636.1:p.Ser827Ala
ENST00000637904.1:c.2638T>G	ENSP00000490550.1:p.Ser880Ala
ENST00000647938.1:c.4768T>G	ENSP00000498155.1:p.Ser1590Ala
ENST00000346085.9:c.4768T>G	ENSP00000344546.4:p.Ser1590Ala
ENST00000350026.9:c.4729T>G	ENSP00000055163.7:p.Ser1577Ala
ENST00000414678.6:c.3295T>G	ENSP00000412835.2:p.Ser1099Ala
NM_017519.2:c.4729T>G	NP_059989.2:p.Ser1577Ala
NM_020732.3:c.4768T>G	NP_065783.3:p.Ser1590Ala
XM_005267069.3:c.4888T>G	XP_005267126.2:p.Ser1630Ala
XM_011535984.1:c.3967T>G	XP_011534286.1:p.Ser1323Ala
XM_011535985.1:c.3787T>G	XP_011534287.1:p.Ser1263Ala
XM_011535986.1:c.3547T>G	XP_011534288.1:p.Ser1183Ala
XM_011535987.1:c.3166T>G	XP_011534289.1:p.Ser1056Ala
XM_011535988.1:c.2029T>G	XP_011534290.1:p.Ser677Ala
NM_001346813.1:c.4888T>G	NP_001333742.1:p.Ser1630Ala
NM_001363725.1:c.2638T>G	NP_001350654.1:p.Ser880Ala
XM_011535984.2:c.5098T>G	XP_011534286.2:p.Ser1700Ala
XM_011535988.3:c.2029T>G	XP_011534290.1:p.Ser677Ala
XM_017011103.2:c.4999T>G	XP_016866592.1:p.Ser1667Ala
XM_017011104.1:c.4969T>G	XP_016866593.1:p.Ser1657Ala
XM_017011105.2:c.4939T>G	XP_016866594.1:p.Ser1647Ala
XM_017011106.2:c.4810T>G	XP_016866595.1:p.Ser1604Ala
XM_017011107.2:c.4789T>G	XP_016866596.1:p.Ser1597Ala
XR_002956289.1:n.5084T>G
NM_001363725.2:c.2638T>G	NP_001350654.1:p.Ser880Ala
NM_001371656.1:c.5017T>G	NP_001358585.1:p.Ser1673Ala
NM_001374820.1:c.5017T>G	NP_001361749.1:p.Ser1673Ala
NM_001374828.1:c.5137T>G MANE Select	NP_001361757.1:p.Ser1713Ala
NM_017519.3:c.4978T>G	NP_059989.3:p.Ser1660Ala