Canonical Allele Identifier: CA366241310

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128373621
• MyVariant Identifiers: chr6:g.157522092C>G (hg19) ; chr6:g.157200958C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200958C>G , CM000668.2:g.157200958C>G	GRCh38
NC_000006.11:g.157522092C>G , CM000668.1:g.157522092C>G	GRCh37
NC_000006.10:g.157563784C>G	NCBI36
NG_032093.1:g.428029C>G
NG_032093.2:g.428029C>G
NG_066624.1:g.429933C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4574C>G	ENSP00000055163.8:p.Ser1525Cys
ENST00000414678.8:c.4643C>G	ENSP00000412835.3:p.Ser1548Cys
ENST00000637015.2:c.4862C>G	ENSP00000489729.2:p.Ser1621Cys
ENST00000346085.10:c.4613C>G	ENSP00000344546.5:p.Ser1538Cys
ENST00000350026.10:c.4325C>G	ENSP00000055163.7:p.Ser1442Cys
ENST00000414678.7:c.2891C>G	ENSP00000412835.2:p.Ser964Cys
ENST00000635849.1:c.2054C>G	ENSP00000490948.1:p.Ser685Cys
ENST00000635957.1:c.1685C>G	ENSP00000490385.1:p.Ser562Cys
ENST00000636227.1:n.3196C>G
ENST00000636254.1:n.653C>G
ENST00000636930.2:c.4733C>G MANE Select	ENSP00000490491.2:p.Ser1578Cys
ENST00000636940.1:n.2730C>G
ENST00000637015.1:c.2101C>G
ENST00000637568.1:c.2015C>G
ENST00000637741.1:n.1399C>G
ENST00000637810.1:c.2075C>G	ENSP00000489636.1:p.Ser692Cys
ENST00000637904.1:c.2234C>G	ENSP00000490550.1:p.Ser745Cys
ENST00000647938.1:c.4364C>G	ENSP00000498155.1:p.Ser1455Cys
ENST00000346085.9:c.4364C>G	ENSP00000344546.4:p.Ser1455Cys
ENST00000350026.9:c.4325C>G	ENSP00000055163.7:p.Ser1442Cys
ENST00000414678.6:c.2891C>G	ENSP00000412835.2:p.Ser964Cys
NM_017519.2:c.4325C>G	NP_059989.2:p.Ser1442Cys
NM_020732.3:c.4364C>G	NP_065783.3:p.Ser1455Cys
XM_005267069.3:c.4484C>G	XP_005267126.2:p.Ser1495Cys
XM_011535984.1:c.3563C>G	XP_011534286.1:p.Ser1188Cys
XM_011535985.1:c.3383C>G	XP_011534287.1:p.Ser1128Cys
XM_011535986.1:c.3143C>G	XP_011534288.1:p.Ser1048Cys
XM_011535987.1:c.2762C>G	XP_011534289.1:p.Ser921Cys
XM_011535988.1:c.1625C>G	XP_011534290.1:p.Ser542Cys
NM_001346813.1:c.4484C>G	NP_001333742.1:p.Ser1495Cys
NM_001363725.1:c.2234C>G	NP_001350654.1:p.Ser745Cys
XM_011535984.2:c.4694C>G	XP_011534286.2:p.Ser1565Cys
XM_011535988.3:c.1625C>G	XP_011534290.1:p.Ser542Cys
XM_017011103.2:c.4595C>G	XP_016866592.1:p.Ser1532Cys
XM_017011104.1:c.4565C>G	XP_016866593.1:p.Ser1522Cys
XM_017011105.2:c.4535C>G	XP_016866594.1:p.Ser1512Cys
XM_017011106.2:c.4406C>G	XP_016866595.1:p.Ser1469Cys
XM_017011107.2:c.4385C>G	XP_016866596.1:p.Ser1462Cys
XR_002956289.1:n.4680C>G
NM_001363725.2:c.2234C>G	NP_001350654.1:p.Ser745Cys
NM_001371656.1:c.4613C>G	NP_001358585.1:p.Ser1538Cys
NM_001374820.1:c.4613C>G	NP_001361749.1:p.Ser1538Cys
NM_001374828.1:c.4733C>G MANE Select	NP_001361757.1:p.Ser1578Cys
NM_017519.3:c.4574C>G	NP_059989.3:p.Ser1525Cys