Canonical Allele Identifier: CA366241300

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522088T>A (hg19) ; chr6:g.157200954T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200954T>A , CM000668.2:g.157200954T>A	GRCh38
NC_000006.11:g.157522088T>A , CM000668.1:g.157522088T>A	GRCh37
NC_000006.10:g.157563780T>A	NCBI36
NG_032093.1:g.428025T>A
NG_032093.2:g.428025T>A
NG_066624.1:g.429929T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4570T>A	ENSP00000055163.8:p.Ser1524Thr
ENST00000414678.8:c.4639T>A	ENSP00000412835.3:p.Ser1547Thr
ENST00000637015.2:c.4858T>A	ENSP00000489729.2:p.Ser1620Thr
ENST00000346085.10:c.4609T>A	ENSP00000344546.5:p.Ser1537Thr
ENST00000350026.10:c.4321T>A	ENSP00000055163.7:p.Ser1441Thr
ENST00000414678.7:c.2887T>A	ENSP00000412835.2:p.Ser963Thr
ENST00000635849.1:c.2050T>A	ENSP00000490948.1:p.Ser684Thr
ENST00000635957.1:c.1681T>A	ENSP00000490385.1:p.Ser561Thr
ENST00000636227.1:n.3192T>A
ENST00000636254.1:n.649T>A
ENST00000636930.2:c.4729T>A MANE Select	ENSP00000490491.2:p.Ser1577Thr
ENST00000636940.1:n.2726T>A
ENST00000637015.1:c.2097T>A
ENST00000637568.1:c.2011T>A
ENST00000637741.1:n.1395T>A
ENST00000637810.1:c.2071T>A	ENSP00000489636.1:p.Ser691Thr
ENST00000637904.1:c.2230T>A	ENSP00000490550.1:p.Ser744Thr
ENST00000647938.1:c.4360T>A	ENSP00000498155.1:p.Ser1454Thr
ENST00000346085.9:c.4360T>A	ENSP00000344546.4:p.Ser1454Thr
ENST00000350026.9:c.4321T>A	ENSP00000055163.7:p.Ser1441Thr
ENST00000414678.6:c.2887T>A	ENSP00000412835.2:p.Ser963Thr
NM_017519.2:c.4321T>A	NP_059989.2:p.Ser1441Thr
NM_020732.3:c.4360T>A	NP_065783.3:p.Ser1454Thr
XM_005267069.3:c.4480T>A	XP_005267126.2:p.Ser1494Thr
XM_011535984.1:c.3559T>A	XP_011534286.1:p.Ser1187Thr
XM_011535985.1:c.3379T>A	XP_011534287.1:p.Ser1127Thr
XM_011535986.1:c.3139T>A	XP_011534288.1:p.Ser1047Thr
XM_011535987.1:c.2758T>A	XP_011534289.1:p.Ser920Thr
XM_011535988.1:c.1621T>A	XP_011534290.1:p.Ser541Thr
NM_001346813.1:c.4480T>A	NP_001333742.1:p.Ser1494Thr
NM_001363725.1:c.2230T>A	NP_001350654.1:p.Ser744Thr
XM_011535984.2:c.4690T>A	XP_011534286.2:p.Ser1564Thr
XM_011535988.3:c.1621T>A	XP_011534290.1:p.Ser541Thr
XM_017011103.2:c.4591T>A	XP_016866592.1:p.Ser1531Thr
XM_017011104.1:c.4561T>A	XP_016866593.1:p.Ser1521Thr
XM_017011105.2:c.4531T>A	XP_016866594.1:p.Ser1511Thr
XM_017011106.2:c.4402T>A	XP_016866595.1:p.Ser1468Thr
XM_017011107.2:c.4381T>A	XP_016866596.1:p.Ser1461Thr
XR_002956289.1:n.4676T>A
NM_001363725.2:c.2230T>A	NP_001350654.1:p.Ser744Thr
NM_001371656.1:c.4609T>A	NP_001358585.1:p.Ser1537Thr
NM_001374820.1:c.4609T>A	NP_001361749.1:p.Ser1537Thr
NM_001374828.1:c.4729T>A MANE Select	NP_001361757.1:p.Ser1577Thr
NM_017519.3:c.4570T>A	NP_059989.3:p.Ser1524Thr