Canonical Allele Identifier: CA366241117

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522005C>A (hg19) ; chr6:g.157200871C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200871C>A , CM000668.2:g.157200871C>A	GRCh38
NC_000006.11:g.157522005C>A , CM000668.1:g.157522005C>A	GRCh37
NC_000006.10:g.157563697C>A	NCBI36
NG_032093.1:g.427942C>A
NG_032093.2:g.427942C>A
NG_066624.1:g.429846C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4487C>A	ENSP00000055163.8:p.Pro1496His
ENST00000414678.8:c.4556C>A	ENSP00000412835.3:p.Pro1519His
ENST00000637015.2:c.4775C>A	ENSP00000489729.2:p.Pro1592His
ENST00000346085.10:c.4526C>A	ENSP00000344546.5:p.Pro1509His
ENST00000350026.10:c.4238C>A	ENSP00000055163.7:p.Pro1413His
ENST00000414678.7:c.2804C>A	ENSP00000412835.2:p.Pro935His
ENST00000635849.1:c.1967C>A	ENSP00000490948.1:p.Pro656His
ENST00000635957.1:c.1598C>A	ENSP00000490385.1:p.Pro533His
ENST00000636227.1:n.3109C>A
ENST00000636254.1:n.566C>A
ENST00000636930.2:c.4646C>A MANE Select	ENSP00000490491.2:p.Pro1549His
ENST00000636940.1:n.2643C>A
ENST00000637015.1:c.2014C>A
ENST00000637568.1:c.1928C>A
ENST00000637741.1:n.1312C>A
ENST00000637810.1:c.1988C>A	ENSP00000489636.1:p.Pro663His
ENST00000637904.1:c.2147C>A	ENSP00000490550.1:p.Pro716His
ENST00000647938.1:c.4277C>A	ENSP00000498155.1:p.Pro1426His
ENST00000346085.9:c.4277C>A	ENSP00000344546.4:p.Pro1426His
ENST00000350026.9:c.4238C>A	ENSP00000055163.7:p.Pro1413His
ENST00000414678.6:c.2804C>A	ENSP00000412835.2:p.Pro935His
NM_017519.2:c.4238C>A	NP_059989.2:p.Pro1413His
NM_020732.3:c.4277C>A	NP_065783.3:p.Pro1426His
XM_005267069.3:c.4397C>A	XP_005267126.2:p.Pro1466His
XM_011535984.1:c.3476C>A	XP_011534286.1:p.Pro1159His
XM_011535985.1:c.3296C>A	XP_011534287.1:p.Pro1099His
XM_011535986.1:c.3056C>A	XP_011534288.1:p.Pro1019His
XM_011535987.1:c.2675C>A	XP_011534289.1:p.Pro892His
XM_011535988.1:c.1538C>A	XP_011534290.1:p.Pro513His
NM_001346813.1:c.4397C>A	NP_001333742.1:p.Pro1466His
NM_001363725.1:c.2147C>A	NP_001350654.1:p.Pro716His
XM_011535984.2:c.4607C>A	XP_011534286.2:p.Pro1536His
XM_011535988.3:c.1538C>A	XP_011534290.1:p.Pro513His
XM_017011103.2:c.4508C>A	XP_016866592.1:p.Pro1503His
XM_017011104.1:c.4478C>A	XP_016866593.1:p.Pro1493His
XM_017011105.2:c.4448C>A	XP_016866594.1:p.Pro1483His
XM_017011106.2:c.4319C>A	XP_016866595.1:p.Pro1440His
XM_017011107.2:c.4298C>A	XP_016866596.1:p.Pro1433His
XR_002956289.1:n.4593C>A
NM_001363725.2:c.2147C>A	NP_001350654.1:p.Pro716His
NM_001371656.1:c.4526C>A	NP_001358585.1:p.Pro1509His
NM_001374820.1:c.4526C>A	NP_001361749.1:p.Pro1509His
NM_001374828.1:c.4646C>A MANE Select	NP_001361757.1:p.Pro1549His
NM_017519.3:c.4487C>A	NP_059989.3:p.Pro1496His