Canonical Allele Identifier: CA452978350

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128375970
• COSMIC: COSM4006182 ; COSM4006183
• MyVariant Identifiers: chr6:g.157522465G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201331G>A , CM000668.2:g.157201331G>A	GRCh38
NC_000006.11:g.157522465G>A , CM000668.1:g.157522465G>A	GRCh37
NC_000006.10:g.157564157G>A	NCBI36
NG_032093.1:g.428402G>A
NG_032093.2:g.428402G>A
NG_066624.1:g.430306G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4947G>A	ENSP00000055163.8:p.Lys1649=
ENST00000414678.8:c.5016G>A	ENSP00000412835.3:p.Lys1672=
ENST00000637015.2:c.5235G>A	ENSP00000489729.2:p.Lys1745=
ENST00000346085.10:c.4986G>A	ENSP00000344546.5:p.Lys1662=
ENST00000350026.10:c.4698G>A	ENSP00000055163.7:p.Lys1566=
ENST00000414678.7:c.3264G>A	ENSP00000412835.2:p.Lys1088=
ENST00000635849.1:c.2427G>A	ENSP00000490948.1:p.Lys809=
ENST00000635957.1:c.2058G>A	ENSP00000490385.1:p.Lys686=
ENST00000636227.1:n.3569G>A
ENST00000636254.1:n.1026G>A
ENST00000636930.2:c.5106G>A MANE Select	ENSP00000490491.2:p.Lys1702=
ENST00000636940.1:n.3103G>A
ENST00000637015.1:c.2474G>A
ENST00000637568.1:c.2388G>A
ENST00000637741.1:n.1772G>A
ENST00000637810.1:c.2448G>A	ENSP00000489636.1:p.Lys816=
ENST00000637904.1:c.2607G>A	ENSP00000490550.1:p.Lys869=
ENST00000647938.1:c.4737G>A	ENSP00000498155.1:p.Lys1579=
ENST00000346085.9:c.4737G>A	ENSP00000344546.4:p.Lys1579=
ENST00000350026.9:c.4698G>A	ENSP00000055163.7:p.Lys1566=
ENST00000414678.6:c.3264G>A	ENSP00000412835.2:p.Lys1088=
NM_017519.2:c.4698G>A	NP_059989.2:p.Lys1566=
NM_020732.3:c.4737G>A	NP_065783.3:p.Lys1579=
XM_005267069.3:c.4857G>A	XP_005267126.2:p.Lys1619=
XM_011535984.1:c.3936G>A	XP_011534286.1:p.Lys1312=
XM_011535985.1:c.3756G>A	XP_011534287.1:p.Lys1252=
XM_011535986.1:c.3516G>A	XP_011534288.1:p.Lys1172=
XM_011535987.1:c.3135G>A	XP_011534289.1:p.Lys1045=
XM_011535988.1:c.1998G>A	XP_011534290.1:p.Lys666=
NM_001346813.1:c.4857G>A	NP_001333742.1:p.Lys1619=
NM_001363725.1:c.2607G>A	NP_001350654.1:p.Lys869=
XM_011535984.2:c.5067G>A	XP_011534286.2:p.Lys1689=
XM_011535988.3:c.1998G>A	XP_011534290.1:p.Lys666=
XM_017011103.2:c.4968G>A	XP_016866592.1:p.Lys1656=
XM_017011104.1:c.4938G>A	XP_016866593.1:p.Lys1646=
XM_017011105.2:c.4908G>A	XP_016866594.1:p.Lys1636=
XM_017011106.2:c.4779G>A	XP_016866595.1:p.Lys1593=
XM_017011107.2:c.4758G>A	XP_016866596.1:p.Lys1586=
XR_002956289.1:n.5053G>A
NM_001363725.2:c.2607G>A	NP_001350654.1:p.Lys869=
NM_001371656.1:c.4986G>A	NP_001358585.1:p.Lys1662=
NM_001374820.1:c.4986G>A	NP_001361749.1:p.Lys1662=
NM_001374828.1:c.5106G>A MANE Select	NP_001361757.1:p.Lys1702=
NM_017519.3:c.4947G>A	NP_059989.3:p.Lys1649=