Canonical Allele Identifier: CA129762

Gene: ARID1B

Linked Data - Expert Curation

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157196221C>T , CM000668.2:g.157196221C>T	GRCh38
NC_000006.11:g.157517355C>T , CM000668.1:g.157517355C>T	GRCh37
NC_000006.10:g.157559047C>T	NCBI36
NG_032093.1:g.423292C>T
NG_032093.2:g.423292C>T
NG_066624.1:g.425196C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4129C>T	ENSP00000055163.8:p.Gln1377Ter
ENST00000414678.8:c.4198C>T	ENSP00000412835.3:p.Gln1400Ter
ENST00000637015.2:c.4417C>T	ENSP00000489729.2:p.Gln1473Ter
ENST00000346085.10:c.4168C>T	ENSP00000344546.5:p.Gln1390Ter
ENST00000350026.10:c.3880C>T	ENSP00000055163.7:p.Gln1294Ter
ENST00000414678.7:c.2446C>T	ENSP00000412835.2:p.Gln816Ter
ENST00000635849.1:c.1609C>T	ENSP00000490948.1:p.Gln537Ter
ENST00000635957.1:c.1240C>T	ENSP00000490385.1:p.Gln414Ter
ENST00000636227.1:n.2751C>T
ENST00000636930.2:c.4288C>T MANE Select	ENSP00000490491.2:p.Gln1430Ter
ENST00000636940.1:n.2285C>T
ENST00000637015.1:c.1656C>T
ENST00000637568.1:c.1570C>T
ENST00000637741.1:n.954C>T
ENST00000637810.1:c.1630C>T	ENSP00000489636.1:p.Gln544Ter
ENST00000637904.1:c.1789C>T	ENSP00000490550.1:p.Gln597Ter
ENST00000647938.1:c.3919C>T	ENSP00000498155.1:p.Gln1307Ter
ENST00000346085.9:c.3919C>T	ENSP00000344546.4:p.Gln1307Ter
ENST00000350026.9:c.3880C>T	ENSP00000055163.7:p.Gln1294Ter
ENST00000414678.6:c.2446C>T	ENSP00000412835.2:p.Gln816Ter
NM_017519.2:c.3880C>T	NP_059989.2:p.Gln1294Ter
NM_020732.3:c.3919C>T	NP_065783.3:p.Gln1307Ter
XM_005267069.3:c.4039C>T	XP_005267126.2:p.Gln1347Ter
XM_011535984.1:c.3118C>T	XP_011534286.1:p.Gln1040Ter
XM_011535985.1:c.2938C>T	XP_011534287.1:p.Gln980Ter
XM_011535986.1:c.2698C>T	XP_011534288.1:p.Gln900Ter
XM_011535987.1:c.2317C>T	XP_011534289.1:p.Gln773Ter
XM_011535988.1:c.1180C>T	XP_011534290.1:p.Gln394Ter
NM_001346813.1:c.4039C>T	NP_001333742.1:p.Gln1347Ter
NM_001363725.1:c.1789C>T	NP_001350654.1:p.Gln597Ter
XM_011535984.2:c.4249C>T	XP_011534286.2:p.Gln1417Ter
XM_011535988.3:c.1180C>T	XP_011534290.1:p.Gln394Ter
XM_017011103.2:c.4150C>T	XP_016866592.1:p.Gln1384Ter
XM_017011104.1:c.4120C>T	XP_016866593.1:p.Gln1374Ter
XM_017011105.2:c.4090C>T	XP_016866594.1:p.Gln1364Ter
XM_017011106.2:c.3961C>T	XP_016866595.1:p.Gln1321Ter
XM_017011107.2:c.3940C>T	XP_016866596.1:p.Gln1314Ter
XR_002956289.1:n.4332C>T
NM_001363725.2:c.1789C>T	NP_001350654.1:p.Gln597Ter
NM_001371656.1:c.4168C>T	NP_001358585.1:p.Gln1390Ter
NM_001374820.1:c.4168C>T	NP_001361749.1:p.Gln1390Ter
NM_001374828.1:c.4288C>T MANE Select	NP_001361757.1:p.Gln1430Ter
NM_017519.3:c.4129C>T	NP_059989.3:p.Gln1377Ter