Canonical Allele Identifier: CA366242405

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522419A>C (hg19) ; chr6:g.157201285A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201285A>C , CM000668.2:g.157201285A>C	GRCh38
NC_000006.11:g.157522419A>C , CM000668.1:g.157522419A>C	GRCh37
NC_000006.10:g.157564111A>C	NCBI36
NG_032093.1:g.428356A>C
NG_032093.2:g.428356A>C
NG_066624.1:g.430260A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4901A>C	ENSP00000055163.8:p.Glu1634Ala
ENST00000414678.8:c.4970A>C	ENSP00000412835.3:p.Glu1657Ala
ENST00000637015.2:c.5189A>C	ENSP00000489729.2:p.Glu1730Ala
ENST00000346085.10:c.4940A>C	ENSP00000344546.5:p.Glu1647Ala
ENST00000350026.10:c.4652A>C	ENSP00000055163.7:p.Glu1551Ala
ENST00000414678.7:c.3218A>C	ENSP00000412835.2:p.Glu1073Ala
ENST00000635849.1:c.2381A>C	ENSP00000490948.1:p.Glu794Ala
ENST00000635957.1:c.2012A>C	ENSP00000490385.1:p.Glu671Ala
ENST00000636227.1:n.3523A>C
ENST00000636254.1:n.980A>C
ENST00000636930.2:c.5060A>C MANE Select	ENSP00000490491.2:p.Glu1687Ala
ENST00000636940.1:n.3057A>C
ENST00000637015.1:c.2428A>C
ENST00000637568.1:c.2342A>C
ENST00000637741.1:n.1726A>C
ENST00000637810.1:c.2402A>C	ENSP00000489636.1:p.Glu801Ala
ENST00000637904.1:c.2561A>C	ENSP00000490550.1:p.Glu854Ala
ENST00000647938.1:c.4691A>C	ENSP00000498155.1:p.Glu1564Ala
ENST00000346085.9:c.4691A>C	ENSP00000344546.4:p.Glu1564Ala
ENST00000350026.9:c.4652A>C	ENSP00000055163.7:p.Glu1551Ala
ENST00000414678.6:c.3218A>C	ENSP00000412835.2:p.Glu1073Ala
NM_017519.2:c.4652A>C	NP_059989.2:p.Glu1551Ala
NM_020732.3:c.4691A>C	NP_065783.3:p.Glu1564Ala
XM_005267069.3:c.4811A>C	XP_005267126.2:p.Glu1604Ala
XM_011535984.1:c.3890A>C	XP_011534286.1:p.Glu1297Ala
XM_011535985.1:c.3710A>C	XP_011534287.1:p.Glu1237Ala
XM_011535986.1:c.3470A>C	XP_011534288.1:p.Glu1157Ala
XM_011535987.1:c.3089A>C	XP_011534289.1:p.Glu1030Ala
XM_011535988.1:c.1952A>C	XP_011534290.1:p.Glu651Ala
NM_001346813.1:c.4811A>C	NP_001333742.1:p.Glu1604Ala
NM_001363725.1:c.2561A>C	NP_001350654.1:p.Glu854Ala
XM_011535984.2:c.5021A>C	XP_011534286.2:p.Glu1674Ala
XM_011535988.3:c.1952A>C	XP_011534290.1:p.Glu651Ala
XM_017011103.2:c.4922A>C	XP_016866592.1:p.Glu1641Ala
XM_017011104.1:c.4892A>C	XP_016866593.1:p.Glu1631Ala
XM_017011105.2:c.4862A>C	XP_016866594.1:p.Glu1621Ala
XM_017011106.2:c.4733A>C	XP_016866595.1:p.Glu1578Ala
XM_017011107.2:c.4712A>C	XP_016866596.1:p.Glu1571Ala
XR_002956289.1:n.5007A>C
NM_001363725.2:c.2561A>C	NP_001350654.1:p.Glu854Ala
NM_001371656.1:c.4940A>C	NP_001358585.1:p.Glu1647Ala
NM_001374820.1:c.4940A>C	NP_001361749.1:p.Glu1647Ala
NM_001374828.1:c.5060A>C MANE Select	NP_001361757.1:p.Glu1687Ala
NM_017519.3:c.4901A>C	NP_059989.3:p.Glu1634Ala