Canonical Allele Identifier: CA452780783

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128317328
• MyVariant Identifiers: chr6:g.157502225T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181091T>A , CM000668.2:g.157181091T>A	GRCh38
NC_000006.11:g.157502225T>A , CM000668.1:g.157502225T>A	GRCh37
NC_000006.10:g.157543917T>A	NCBI36
NG_032093.1:g.408162T>A
NG_032093.2:g.408162T>A
NG_066624.1:g.410066T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3468T>A	ENSP00000055163.8:p.Pro1156=
ENST00000414678.8:c.3537T>A	ENSP00000412835.3:p.Pro1179=
ENST00000637015.2:c.3756T>A	ENSP00000489729.2:p.Pro1252=
ENST00000319584.11:c.1641T>A	ENSP00000313006.7:p.Pro547=
ENST00000346085.10:c.3507T>A	ENSP00000344546.5:p.Pro1169=
ENST00000350026.10:c.3219T>A	ENSP00000055163.7:p.Pro1073=
ENST00000414678.7:c.1785T>A	ENSP00000412835.2:p.Pro595=
ENST00000635849.1:c.948T>A	ENSP00000490948.1:p.Pro316=
ENST00000635957.1:c.582T>A	ENSP00000490385.1:p.Pro194=
ENST00000636930.2:c.3627T>A MANE Select	ENSP00000490491.2:p.Pro1209=
ENST00000636940.1:n.1624T>A
ENST00000637015.1:c.995T>A
ENST00000637568.1:c.909T>A
ENST00000637741.1:n.293T>A
ENST00000637810.1:c.969T>A	ENSP00000489636.1:p.Pro323=
ENST00000637904.1:c.1128T>A	ENSP00000490550.1:p.Pro376=
ENST00000647938.1:c.3258T>A	ENSP00000498155.1:p.Pro1086=
ENST00000319584.10:c.1644T>A	ENSP00000313006.6:p.Pro548=
ENST00000346085.9:c.3258T>A	ENSP00000344546.4:p.Pro1086=
ENST00000350026.9:c.3219T>A	ENSP00000055163.7:p.Pro1073=
ENST00000400790.3:c.420T>A	ENSP00000383596.3:p.Pro140=
ENST00000414678.6:c.1785T>A	ENSP00000412835.2:p.Pro595=
ENST00000478761.3:c.829T>A
NM_017519.2:c.3219T>A	NP_059989.2:p.Pro1073=
NM_020732.3:c.3258T>A	NP_065783.3:p.Pro1086=
XM_005267069.3:c.3378T>A	XP_005267126.2:p.Pro1126=
XM_011535984.1:c.2457T>A	XP_011534286.1:p.Pro819=
XM_011535985.1:c.2277T>A	XP_011534287.1:p.Pro759=
XM_011535986.1:c.2037T>A	XP_011534288.1:p.Pro679=
XM_011535987.1:c.1656T>A	XP_011534289.1:p.Pro552=
XM_011535988.1:c.519T>A	XP_011534290.1:p.Pro173=
NM_001346813.1:c.3378T>A	NP_001333742.1:p.Pro1126=
NM_001363725.1:c.1128T>A	NP_001350654.1:p.Pro376=
XM_011535984.2:c.3588T>A	XP_011534286.2:p.Pro1196=
XM_011535988.3:c.519T>A	XP_011534290.1:p.Pro173=
XM_017011103.2:c.3489T>A	XP_016866592.1:p.Pro1163=
XM_017011104.1:c.3459T>A	XP_016866593.1:p.Pro1153=
XM_017011105.2:c.3429T>A	XP_016866594.1:p.Pro1143=
XM_017011106.2:c.3300T>A	XP_016866595.1:p.Pro1100=
XM_017011107.2:c.3279T>A	XP_016866596.1:p.Pro1093=
XR_002956289.1:n.3671T>A
NM_001363725.2:c.1128T>A	NP_001350654.1:p.Pro376=
NM_001371656.1:c.3507T>A	NP_001358585.1:p.Pro1169=
NM_001374820.1:c.3507T>A	NP_001361749.1:p.Pro1169=
NM_001374828.1:c.3627T>A MANE Select	NP_001361757.1:p.Pro1209=
NM_017519.3:c.3468T>A	NP_059989.3:p.Pro1156=