Canonical Allele Identifier: CA366234781

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128339625
• COSMIC: COSM1441819 ; COSM1441820
• MyVariant Identifiers: chr6:g.157511191C>T (hg19) ; chr6:g.157190057C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190057C>T , CM000668.2:g.157190057C>T	GRCh38
NC_000006.11:g.157511191C>T , CM000668.1:g.157511191C>T	GRCh37
NC_000006.10:g.157552883C>T	NCBI36
NG_032093.1:g.417128C>T
NG_032093.2:g.417128C>T
NG_066624.1:g.419032C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3919C>T	ENSP00000055163.8:p.His1307Tyr
ENST00000414678.8:c.3988C>T	ENSP00000412835.3:p.His1330Tyr
ENST00000637015.2:c.4207C>T	ENSP00000489729.2:p.His1403Tyr
ENST00000346085.10:c.3958C>T	ENSP00000344546.5:p.His1320Tyr
ENST00000350026.10:c.3670C>T	ENSP00000055163.7:p.His1224Tyr
ENST00000414678.7:c.2236C>T	ENSP00000412835.2:p.His746Tyr
ENST00000635849.1:c.1399C>T	ENSP00000490948.1:p.His467Tyr
ENST00000635957.1:c.1030C>T	ENSP00000490385.1:p.His344Tyr
ENST00000636930.2:c.4078C>T MANE Select	ENSP00000490491.2:p.His1360Tyr
ENST00000636940.1:n.2075C>T
ENST00000637015.1:c.1446C>T
ENST00000637568.1:c.1360C>T
ENST00000637741.1:n.744C>T
ENST00000637810.1:c.1420C>T	ENSP00000489636.1:p.His474Tyr
ENST00000637904.1:c.1579C>T	ENSP00000490550.1:p.His527Tyr
ENST00000647938.1:c.3709C>T	ENSP00000498155.1:p.His1237Tyr
ENST00000346085.9:c.3709C>T	ENSP00000344546.4:p.His1237Tyr
ENST00000350026.9:c.3670C>T	ENSP00000055163.7:p.His1224Tyr
ENST00000414678.6:c.2236C>T	ENSP00000412835.2:p.His746Tyr
NM_017519.2:c.3670C>T	NP_059989.2:p.His1224Tyr
NM_020732.3:c.3709C>T	NP_065783.3:p.His1237Tyr
XM_005267069.3:c.3829C>T	XP_005267126.2:p.His1277Tyr
XM_011535984.1:c.2908C>T	XP_011534286.1:p.His970Tyr
XM_011535985.1:c.2728C>T	XP_011534287.1:p.His910Tyr
XM_011535986.1:c.2488C>T	XP_011534288.1:p.His830Tyr
XM_011535987.1:c.2107C>T	XP_011534289.1:p.His703Tyr
XM_011535988.1:c.970C>T	XP_011534290.1:p.His324Tyr
NM_001346813.1:c.3829C>T	NP_001333742.1:p.His1277Tyr
NM_001363725.1:c.1579C>T	NP_001350654.1:p.His527Tyr
XM_011535984.2:c.4039C>T	XP_011534286.2:p.His1347Tyr
XM_011535988.3:c.970C>T	XP_011534290.1:p.His324Tyr
XM_017011103.2:c.3940C>T	XP_016866592.1:p.His1314Tyr
XM_017011104.1:c.3910C>T	XP_016866593.1:p.His1304Tyr
XM_017011105.2:c.3880C>T	XP_016866594.1:p.His1294Tyr
XM_017011106.2:c.3751C>T	XP_016866595.1:p.His1251Tyr
XM_017011107.2:c.3730C>T	XP_016866596.1:p.His1244Tyr
XR_002956289.1:n.4122C>T
NM_001363725.2:c.1579C>T	NP_001350654.1:p.His527Tyr
NM_001371656.1:c.3958C>T	NP_001358585.1:p.His1320Tyr
NM_001374820.1:c.3958C>T	NP_001361749.1:p.His1320Tyr
NM_001374828.1:c.4078C>T MANE Select	NP_001361757.1:p.His1360Tyr
NM_017519.3:c.3919C>T	NP_059989.3:p.His1307Tyr