Canonical Allele Identifier: CA366234928

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157511203T>A (hg19) ; chr6:g.157190069T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190069T>A , CM000668.2:g.157190069T>A	GRCh38
NC_000006.11:g.157511203T>A , CM000668.1:g.157511203T>A	GRCh37
NC_000006.10:g.157552895T>A	NCBI36
NG_032093.1:g.417140T>A
NG_032093.2:g.417140T>A
NG_066624.1:g.419044T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3931T>A	ENSP00000055163.8:p.Ser1311Thr
ENST00000414678.8:c.4000T>A	ENSP00000412835.3:p.Ser1334Thr
ENST00000637015.2:c.4219T>A	ENSP00000489729.2:p.Ser1407Thr
ENST00000346085.10:c.3970T>A	ENSP00000344546.5:p.Ser1324Thr
ENST00000350026.10:c.3682T>A	ENSP00000055163.7:p.Ser1228Thr
ENST00000414678.7:c.2248T>A	ENSP00000412835.2:p.Ser750Thr
ENST00000635849.1:c.1411T>A	ENSP00000490948.1:p.Ser471Thr
ENST00000635957.1:c.1042T>A	ENSP00000490385.1:p.Ser348Thr
ENST00000636930.2:c.4090T>A MANE Select	ENSP00000490491.2:p.Ser1364Thr
ENST00000636940.1:n.2087T>A
ENST00000637015.1:c.1458T>A
ENST00000637568.1:c.1372T>A
ENST00000637741.1:n.756T>A
ENST00000637810.1:c.1432T>A	ENSP00000489636.1:p.Ser478Thr
ENST00000637904.1:c.1591T>A	ENSP00000490550.1:p.Ser531Thr
ENST00000647938.1:c.3721T>A	ENSP00000498155.1:p.Ser1241Thr
ENST00000346085.9:c.3721T>A	ENSP00000344546.4:p.Ser1241Thr
ENST00000350026.9:c.3682T>A	ENSP00000055163.7:p.Ser1228Thr
ENST00000414678.6:c.2248T>A	ENSP00000412835.2:p.Ser750Thr
NM_017519.2:c.3682T>A	NP_059989.2:p.Ser1228Thr
NM_020732.3:c.3721T>A	NP_065783.3:p.Ser1241Thr
XM_005267069.3:c.3841T>A	XP_005267126.2:p.Ser1281Thr
XM_011535984.1:c.2920T>A	XP_011534286.1:p.Ser974Thr
XM_011535985.1:c.2740T>A	XP_011534287.1:p.Ser914Thr
XM_011535986.1:c.2500T>A	XP_011534288.1:p.Ser834Thr
XM_011535987.1:c.2119T>A	XP_011534289.1:p.Ser707Thr
XM_011535988.1:c.982T>A	XP_011534290.1:p.Ser328Thr
NM_001346813.1:c.3841T>A	NP_001333742.1:p.Ser1281Thr
NM_001363725.1:c.1591T>A	NP_001350654.1:p.Ser531Thr
XM_011535984.2:c.4051T>A	XP_011534286.2:p.Ser1351Thr
XM_011535988.3:c.982T>A	XP_011534290.1:p.Ser328Thr
XM_017011103.2:c.3952T>A	XP_016866592.1:p.Ser1318Thr
XM_017011104.1:c.3922T>A	XP_016866593.1:p.Ser1308Thr
XM_017011105.2:c.3892T>A	XP_016866594.1:p.Ser1298Thr
XM_017011106.2:c.3763T>A	XP_016866595.1:p.Ser1255Thr
XM_017011107.2:c.3742T>A	XP_016866596.1:p.Ser1248Thr
XR_002956289.1:n.4134T>A
NM_001363725.2:c.1591T>A	NP_001350654.1:p.Ser531Thr
NM_001371656.1:c.3970T>A	NP_001358585.1:p.Ser1324Thr
NM_001374820.1:c.3970T>A	NP_001361749.1:p.Ser1324Thr
NM_001374828.1:c.4090T>A MANE Select	NP_001361757.1:p.Ser1364Thr
NM_017519.3:c.3931T>A	NP_059989.3:p.Ser1311Thr