Canonical Allele Identifier: CA366228543

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157502307G>A (hg19) ; chr6:g.157181173G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181173G>A , CM000668.2:g.157181173G>A	GRCh38
NC_000006.11:g.157502307G>A , CM000668.1:g.157502307G>A	GRCh37
NC_000006.10:g.157543999G>A	NCBI36
NG_032093.1:g.408244G>A
NG_032093.2:g.408244G>A
NG_066624.1:g.410148G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3550G>A	ENSP00000055163.8:p.Ala1184Thr
ENST00000414678.8:c.3619G>A	ENSP00000412835.3:p.Ala1207Thr
ENST00000637015.2:c.3838G>A	ENSP00000489729.2:p.Ala1280Thr
ENST00000319584.11:c.1723G>A	ENSP00000313006.7:p.Ala575Thr
ENST00000346085.10:c.3589G>A	ENSP00000344546.5:p.Ala1197Thr
ENST00000350026.10:c.3301G>A	ENSP00000055163.7:p.Ala1101Thr
ENST00000414678.7:c.1867G>A	ENSP00000412835.2:p.Ala623Thr
ENST00000635849.1:c.1030G>A	ENSP00000490948.1:p.Ala344Thr
ENST00000635957.1:c.664G>A	ENSP00000490385.1:p.Ala222Thr
ENST00000636930.2:c.3709G>A MANE Select	ENSP00000490491.2:p.Ala1237Thr
ENST00000636940.1:n.1706G>A
ENST00000637015.1:c.1077G>A
ENST00000637568.1:c.991G>A
ENST00000637741.1:n.375G>A
ENST00000637810.1:c.1051G>A	ENSP00000489636.1:p.Ala351Thr
ENST00000637904.1:c.1210G>A	ENSP00000490550.1:p.Ala404Thr
ENST00000647938.1:c.3340G>A	ENSP00000498155.1:p.Ala1114Thr
ENST00000319584.10:c.1726G>A	ENSP00000313006.6:p.Ala576Thr
ENST00000346085.9:c.3340G>A	ENSP00000344546.4:p.Ala1114Thr
ENST00000350026.9:c.3301G>A	ENSP00000055163.7:p.Ala1101Thr
ENST00000400790.3:c.502G>A	ENSP00000383596.3:p.Ala168Thr
ENST00000414678.6:c.1867G>A	ENSP00000412835.2:p.Ala623Thr
ENST00000478761.3:c.911G>A
NM_017519.2:c.3301G>A	NP_059989.2:p.Ala1101Thr
NM_020732.3:c.3340G>A	NP_065783.3:p.Ala1114Thr
XM_005267069.3:c.3460G>A	XP_005267126.2:p.Ala1154Thr
XM_011535984.1:c.2539G>A	XP_011534286.1:p.Ala847Thr
XM_011535985.1:c.2359G>A	XP_011534287.1:p.Ala787Thr
XM_011535986.1:c.2119G>A	XP_011534288.1:p.Ala707Thr
XM_011535987.1:c.1738G>A	XP_011534289.1:p.Ala580Thr
XM_011535988.1:c.601G>A	XP_011534290.1:p.Ala201Thr
NM_001346813.1:c.3460G>A	NP_001333742.1:p.Ala1154Thr
NM_001363725.1:c.1210G>A	NP_001350654.1:p.Ala404Thr
XM_011535984.2:c.3670G>A	XP_011534286.2:p.Ala1224Thr
XM_011535988.3:c.601G>A	XP_011534290.1:p.Ala201Thr
XM_017011103.2:c.3571G>A	XP_016866592.1:p.Ala1191Thr
XM_017011104.1:c.3541G>A	XP_016866593.1:p.Ala1181Thr
XM_017011105.2:c.3511G>A	XP_016866594.1:p.Ala1171Thr
XM_017011106.2:c.3382G>A	XP_016866595.1:p.Ala1128Thr
XM_017011107.2:c.3361G>A	XP_016866596.1:p.Ala1121Thr
XR_002956289.1:n.3753G>A
NM_001363725.2:c.1210G>A	NP_001350654.1:p.Ala404Thr
NM_001371656.1:c.3589G>A	NP_001358585.1:p.Ala1197Thr
NM_001374820.1:c.3589G>A	NP_001361749.1:p.Ala1197Thr
NM_001374828.1:c.3709G>A MANE Select	NP_001361757.1:p.Ala1237Thr
NM_017519.3:c.3550G>A	NP_059989.3:p.Ala1184Thr