Canonical Allele Identifier: CA366241397

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522130C>A (hg19) ; chr6:g.157200996C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200996C>A , CM000668.2:g.157200996C>A	GRCh38
NC_000006.11:g.157522130C>A , CM000668.1:g.157522130C>A	GRCh37
NC_000006.10:g.157563822C>A	NCBI36
NG_032093.1:g.428067C>A
NG_032093.2:g.428067C>A
NG_066624.1:g.429971C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4612C>A	ENSP00000055163.8:p.Arg1538Ser
ENST00000414678.8:c.4681C>A	ENSP00000412835.3:p.Arg1561Ser
ENST00000637015.2:c.4900C>A	ENSP00000489729.2:p.Arg1634Ser
ENST00000346085.10:c.4651C>A	ENSP00000344546.5:p.Arg1551Ser
ENST00000350026.10:c.4363C>A	ENSP00000055163.7:p.Arg1455Ser
ENST00000414678.7:c.2929C>A	ENSP00000412835.2:p.Arg977Ser
ENST00000635849.1:c.2092C>A	ENSP00000490948.1:p.Arg698Ser
ENST00000635957.1:c.1723C>A	ENSP00000490385.1:p.Arg575Ser
ENST00000636227.1:n.3234C>A
ENST00000636254.1:n.691C>A
ENST00000636930.2:c.4771C>A MANE Select	ENSP00000490491.2:p.Arg1591Ser
ENST00000636940.1:n.2768C>A
ENST00000637015.1:c.2139C>A
ENST00000637568.1:c.2053C>A
ENST00000637741.1:n.1437C>A
ENST00000637810.1:c.2113C>A	ENSP00000489636.1:p.Arg705Ser
ENST00000637904.1:c.2272C>A	ENSP00000490550.1:p.Arg758Ser
ENST00000647938.1:c.4402C>A	ENSP00000498155.1:p.Arg1468Ser
ENST00000346085.9:c.4402C>A	ENSP00000344546.4:p.Arg1468Ser
ENST00000350026.9:c.4363C>A	ENSP00000055163.7:p.Arg1455Ser
ENST00000414678.6:c.2929C>A	ENSP00000412835.2:p.Arg977Ser
NM_017519.2:c.4363C>A	NP_059989.2:p.Arg1455Ser
NM_020732.3:c.4402C>A	NP_065783.3:p.Arg1468Ser
XM_005267069.3:c.4522C>A	XP_005267126.2:p.Arg1508Ser
XM_011535984.1:c.3601C>A	XP_011534286.1:p.Arg1201Ser
XM_011535985.1:c.3421C>A	XP_011534287.1:p.Arg1141Ser
XM_011535986.1:c.3181C>A	XP_011534288.1:p.Arg1061Ser
XM_011535987.1:c.2800C>A	XP_011534289.1:p.Arg934Ser
XM_011535988.1:c.1663C>A	XP_011534290.1:p.Arg555Ser
NM_001346813.1:c.4522C>A	NP_001333742.1:p.Arg1508Ser
NM_001363725.1:c.2272C>A	NP_001350654.1:p.Arg758Ser
XM_011535984.2:c.4732C>A	XP_011534286.2:p.Arg1578Ser
XM_011535988.3:c.1663C>A	XP_011534290.1:p.Arg555Ser
XM_017011103.2:c.4633C>A	XP_016866592.1:p.Arg1545Ser
XM_017011104.1:c.4603C>A	XP_016866593.1:p.Arg1535Ser
XM_017011105.2:c.4573C>A	XP_016866594.1:p.Arg1525Ser
XM_017011106.2:c.4444C>A	XP_016866595.1:p.Arg1482Ser
XM_017011107.2:c.4423C>A	XP_016866596.1:p.Arg1475Ser
XR_002956289.1:n.4718C>A
NM_001363725.2:c.2272C>A	NP_001350654.1:p.Arg758Ser
NM_001371656.1:c.4651C>A	NP_001358585.1:p.Arg1551Ser
NM_001374820.1:c.4651C>A	NP_001361749.1:p.Arg1551Ser
NM_001374828.1:c.4771C>A MANE Select	NP_001361757.1:p.Arg1591Ser
NM_017519.3:c.4612C>A	NP_059989.3:p.Arg1538Ser