Canonical Allele Identifier: CA452978270

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128373758
• MyVariant Identifiers: chr6:g.157522108T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200974T>A , CM000668.2:g.157200974T>A	GRCh38
NC_000006.11:g.157522108T>A , CM000668.1:g.157522108T>A	GRCh37
NC_000006.10:g.157563800T>A	NCBI36
NG_032093.1:g.428045T>A
NG_032093.2:g.428045T>A
NG_066624.1:g.429949T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4590T>A	ENSP00000055163.8:p.Pro1530=
ENST00000414678.8:c.4659T>A	ENSP00000412835.3:p.Pro1553=
ENST00000637015.2:c.4878T>A	ENSP00000489729.2:p.Pro1626=
ENST00000346085.10:c.4629T>A	ENSP00000344546.5:p.Pro1543=
ENST00000350026.10:c.4341T>A	ENSP00000055163.7:p.Pro1447=
ENST00000414678.7:c.2907T>A	ENSP00000412835.2:p.Pro969=
ENST00000635849.1:c.2070T>A	ENSP00000490948.1:p.Pro690=
ENST00000635957.1:c.1701T>A	ENSP00000490385.1:p.Pro567=
ENST00000636227.1:n.3212T>A
ENST00000636254.1:n.669T>A
ENST00000636930.2:c.4749T>A MANE Select	ENSP00000490491.2:p.Pro1583=
ENST00000636940.1:n.2746T>A
ENST00000637015.1:c.2117T>A
ENST00000637568.1:c.2031T>A
ENST00000637741.1:n.1415T>A
ENST00000637810.1:c.2091T>A	ENSP00000489636.1:p.Pro697=
ENST00000637904.1:c.2250T>A	ENSP00000490550.1:p.Pro750=
ENST00000647938.1:c.4380T>A	ENSP00000498155.1:p.Pro1460=
ENST00000346085.9:c.4380T>A	ENSP00000344546.4:p.Pro1460=
ENST00000350026.9:c.4341T>A	ENSP00000055163.7:p.Pro1447=
ENST00000414678.6:c.2907T>A	ENSP00000412835.2:p.Pro969=
NM_017519.2:c.4341T>A	NP_059989.2:p.Pro1447=
NM_020732.3:c.4380T>A	NP_065783.3:p.Pro1460=
XM_005267069.3:c.4500T>A	XP_005267126.2:p.Pro1500=
XM_011535984.1:c.3579T>A	XP_011534286.1:p.Pro1193=
XM_011535985.1:c.3399T>A	XP_011534287.1:p.Pro1133=
XM_011535986.1:c.3159T>A	XP_011534288.1:p.Pro1053=
XM_011535987.1:c.2778T>A	XP_011534289.1:p.Pro926=
XM_011535988.1:c.1641T>A	XP_011534290.1:p.Pro547=
NM_001346813.1:c.4500T>A	NP_001333742.1:p.Pro1500=
NM_001363725.1:c.2250T>A	NP_001350654.1:p.Pro750=
XM_011535984.2:c.4710T>A	XP_011534286.2:p.Pro1570=
XM_011535988.3:c.1641T>A	XP_011534290.1:p.Pro547=
XM_017011103.2:c.4611T>A	XP_016866592.1:p.Pro1537=
XM_017011104.1:c.4581T>A	XP_016866593.1:p.Pro1527=
XM_017011105.2:c.4551T>A	XP_016866594.1:p.Pro1517=
XM_017011106.2:c.4422T>A	XP_016866595.1:p.Pro1474=
XM_017011107.2:c.4401T>A	XP_016866596.1:p.Pro1467=
XR_002956289.1:n.4696T>A
NM_001363725.2:c.2250T>A	NP_001350654.1:p.Pro750=
NM_001371656.1:c.4629T>A	NP_001358585.1:p.Pro1543=
NM_001374820.1:c.4629T>A	NP_001361749.1:p.Pro1543=
NM_001374828.1:c.4749T>A MANE Select	NP_001361757.1:p.Pro1583=
NM_017519.3:c.4590T>A	NP_059989.3:p.Pro1530=