Canonical Allele Identifier: CA366241302

Gene: ARID1B

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4570T>G	ENSP00000055163.8:p.Ser1524Ala
ENST00000414678.8:c.4639T>G	ENSP00000412835.3:p.Ser1547Ala
ENST00000637015.2:c.4858T>G	ENSP00000489729.2:p.Ser1620Ala
ENST00000346085.10:c.4609T>G	ENSP00000344546.5:p.Ser1537Ala
ENST00000350026.10:c.4321T>G	ENSP00000055163.7:p.Ser1441Ala
ENST00000414678.7:c.2887T>G	ENSP00000412835.2:p.Ser963Ala
ENST00000635849.1:c.2050T>G	ENSP00000490948.1:p.Ser684Ala
ENST00000635957.1:c.1681T>G	ENSP00000490385.1:p.Ser561Ala
ENST00000636227.1:n.3192T>G
ENST00000636254.1:n.649T>G
ENST00000636930.2:c.4729T>G MANE Select	ENSP00000490491.2:p.Ser1577Ala
ENST00000636940.1:n.2726T>G
ENST00000637015.1:c.2097T>G
ENST00000637568.1:c.2011T>G
ENST00000637741.1:n.1395T>G
ENST00000637810.1:c.2071T>G	ENSP00000489636.1:p.Ser691Ala
ENST00000637904.1:c.2230T>G	ENSP00000490550.1:p.Ser744Ala
ENST00000647938.1:c.4360T>G	ENSP00000498155.1:p.Ser1454Ala
ENST00000346085.9:c.4360T>G	ENSP00000344546.4:p.Ser1454Ala
ENST00000350026.9:c.4321T>G	ENSP00000055163.7:p.Ser1441Ala
ENST00000414678.6:c.2887T>G	ENSP00000412835.2:p.Ser963Ala
NM_017519.2:c.4321T>G	NP_059989.2:p.Ser1441Ala
NM_020732.3:c.4360T>G	NP_065783.3:p.Ser1454Ala
XM_005267069.3:c.4480T>G	XP_005267126.2:p.Ser1494Ala
XM_011535984.1:c.3559T>G	XP_011534286.1:p.Ser1187Ala
XM_011535985.1:c.3379T>G	XP_011534287.1:p.Ser1127Ala
XM_011535986.1:c.3139T>G	XP_011534288.1:p.Ser1047Ala
XM_011535987.1:c.2758T>G	XP_011534289.1:p.Ser920Ala
XM_011535988.1:c.1621T>G	XP_011534290.1:p.Ser541Ala
NM_001346813.1:c.4480T>G	NP_001333742.1:p.Ser1494Ala
NM_001363725.1:c.2230T>G	NP_001350654.1:p.Ser744Ala
XM_011535984.2:c.4690T>G	XP_011534286.2:p.Ser1564Ala
XM_011535988.3:c.1621T>G	XP_011534290.1:p.Ser541Ala
XM_017011103.2:c.4591T>G	XP_016866592.1:p.Ser1531Ala
XM_017011104.1:c.4561T>G	XP_016866593.1:p.Ser1521Ala
XM_017011105.2:c.4531T>G	XP_016866594.1:p.Ser1511Ala
XM_017011106.2:c.4402T>G	XP_016866595.1:p.Ser1468Ala
XM_017011107.2:c.4381T>G	XP_016866596.1:p.Ser1461Ala
XR_002956289.1:n.4676T>G
NM_001363725.2:c.2230T>G	NP_001350654.1:p.Ser744Ala
NM_001371656.1:c.4609T>G	NP_001358585.1:p.Ser1537Ala
NM_001374820.1:c.4609T>G	NP_001361749.1:p.Ser1537Ala
NM_001374828.1:c.4729T>G MANE Select	NP_001361757.1:p.Ser1577Ala
NM_017519.3:c.4570T>G	NP_059989.3:p.Ser1524Ala