Canonical Allele Identifier: CA366238244

Gene: ARID1B

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4129C>A	ENSP00000055163.8:p.Gln1377Lys
ENST00000414678.8:c.4198C>A	ENSP00000412835.3:p.Gln1400Lys
ENST00000637015.2:c.4417C>A	ENSP00000489729.2:p.Gln1473Lys
ENST00000346085.10:c.4168C>A	ENSP00000344546.5:p.Gln1390Lys
ENST00000350026.10:c.3880C>A	ENSP00000055163.7:p.Gln1294Lys
ENST00000414678.7:c.2446C>A	ENSP00000412835.2:p.Gln816Lys
ENST00000635849.1:c.1609C>A	ENSP00000490948.1:p.Gln537Lys
ENST00000635957.1:c.1240C>A	ENSP00000490385.1:p.Gln414Lys
ENST00000636227.1:n.2751C>A
ENST00000636930.2:c.4288C>A MANE Select	ENSP00000490491.2:p.Gln1430Lys
ENST00000636940.1:n.2285C>A
ENST00000637015.1:c.1656C>A
ENST00000637568.1:c.1570C>A
ENST00000637741.1:n.954C>A
ENST00000637810.1:c.1630C>A	ENSP00000489636.1:p.Gln544Lys
ENST00000637904.1:c.1789C>A	ENSP00000490550.1:p.Gln597Lys
ENST00000647938.1:c.3919C>A	ENSP00000498155.1:p.Gln1307Lys
ENST00000346085.9:c.3919C>A	ENSP00000344546.4:p.Gln1307Lys
ENST00000350026.9:c.3880C>A	ENSP00000055163.7:p.Gln1294Lys
ENST00000414678.6:c.2446C>A	ENSP00000412835.2:p.Gln816Lys
NM_017519.2:c.3880C>A	NP_059989.2:p.Gln1294Lys
NM_020732.3:c.3919C>A	NP_065783.3:p.Gln1307Lys
XM_005267069.3:c.4039C>A	XP_005267126.2:p.Gln1347Lys
XM_011535984.1:c.3118C>A	XP_011534286.1:p.Gln1040Lys
XM_011535985.1:c.2938C>A	XP_011534287.1:p.Gln980Lys
XM_011535986.1:c.2698C>A	XP_011534288.1:p.Gln900Lys
XM_011535987.1:c.2317C>A	XP_011534289.1:p.Gln773Lys
XM_011535988.1:c.1180C>A	XP_011534290.1:p.Gln394Lys
NM_001346813.1:c.4039C>A	NP_001333742.1:p.Gln1347Lys
NM_001363725.1:c.1789C>A	NP_001350654.1:p.Gln597Lys
XM_011535984.2:c.4249C>A	XP_011534286.2:p.Gln1417Lys
XM_011535988.3:c.1180C>A	XP_011534290.1:p.Gln394Lys
XM_017011103.2:c.4150C>A	XP_016866592.1:p.Gln1384Lys
XM_017011104.1:c.4120C>A	XP_016866593.1:p.Gln1374Lys
XM_017011105.2:c.4090C>A	XP_016866594.1:p.Gln1364Lys
XM_017011106.2:c.3961C>A	XP_016866595.1:p.Gln1321Lys
XM_017011107.2:c.3940C>A	XP_016866596.1:p.Gln1314Lys
XR_002956289.1:n.4332C>A
NM_001363725.2:c.1789C>A	NP_001350654.1:p.Gln597Lys
NM_001371656.1:c.4168C>A	NP_001358585.1:p.Gln1390Lys
NM_001374820.1:c.4168C>A	NP_001361749.1:p.Gln1390Lys
NM_001374828.1:c.4288C>A MANE Select	NP_001361757.1:p.Gln1430Lys
NM_017519.3:c.4129C>A	NP_059989.3:p.Gln1377Lys