Canonical Allele Identifier: CA366241736

Gene: ARID1B

Linked Data

• COSMIC: COSM3859985 ; COSM3859986
• MyVariant Identifiers: chr6:g.157522190C>G (hg19) ; chr6:g.157201056C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201056C>G , CM000668.2:g.157201056C>G	GRCh38
NC_000006.11:g.157522190C>G , CM000668.1:g.157522190C>G	GRCh37
NC_000006.10:g.157563882C>G	NCBI36
NG_032093.1:g.428127C>G
NG_032093.2:g.428127C>G
NG_066624.1:g.430031C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.4672C>G	ENSP00000055163.8:p.Pro1558Ala
ENST00000414678.8:c.4741C>G	ENSP00000412835.3:p.Pro1581Ala
ENST00000637015.2:c.4960C>G	ENSP00000489729.2:p.Pro1654Ala
ENST00000346085.10:c.4711C>G	ENSP00000344546.5:p.Pro1571Ala
ENST00000350026.10:c.4423C>G	ENSP00000055163.7:p.Pro1475Ala
ENST00000414678.7:c.2989C>G	ENSP00000412835.2:p.Pro997Ala
ENST00000635849.1:c.2152C>G	ENSP00000490948.1:p.Pro718Ala
ENST00000635957.1:c.1783C>G	ENSP00000490385.1:p.Pro595Ala
ENST00000636227.1:n.3294C>G
ENST00000636254.1:n.751C>G
ENST00000636930.2:c.4831C>G MANE Select	ENSP00000490491.2:p.Pro1611Ala
ENST00000636940.1:n.2828C>G
ENST00000637015.1:c.2199C>G
ENST00000637568.1:c.2113C>G
ENST00000637741.1:n.1497C>G
ENST00000637810.1:c.2173C>G	ENSP00000489636.1:p.Pro725Ala
ENST00000637904.1:c.2332C>G	ENSP00000490550.1:p.Pro778Ala
ENST00000647938.1:c.4462C>G	ENSP00000498155.1:p.Pro1488Ala
ENST00000346085.9:c.4462C>G	ENSP00000344546.4:p.Pro1488Ala
ENST00000350026.9:c.4423C>G	ENSP00000055163.7:p.Pro1475Ala
ENST00000414678.6:c.2989C>G	ENSP00000412835.2:p.Pro997Ala
NM_017519.2:c.4423C>G	NP_059989.2:p.Pro1475Ala
NM_020732.3:c.4462C>G	NP_065783.3:p.Pro1488Ala
XM_005267069.3:c.4582C>G	XP_005267126.2:p.Pro1528Ala
XM_011535984.1:c.3661C>G	XP_011534286.1:p.Pro1221Ala
XM_011535985.1:c.3481C>G	XP_011534287.1:p.Pro1161Ala
XM_011535986.1:c.3241C>G	XP_011534288.1:p.Pro1081Ala
XM_011535987.1:c.2860C>G	XP_011534289.1:p.Pro954Ala
XM_011535988.1:c.1723C>G	XP_011534290.1:p.Pro575Ala
NM_001346813.1:c.4582C>G	NP_001333742.1:p.Pro1528Ala
NM_001363725.1:c.2332C>G	NP_001350654.1:p.Pro778Ala
XM_011535984.2:c.4792C>G	XP_011534286.2:p.Pro1598Ala
XM_011535988.3:c.1723C>G	XP_011534290.1:p.Pro575Ala
XM_017011103.2:c.4693C>G	XP_016866592.1:p.Pro1565Ala
XM_017011104.1:c.4663C>G	XP_016866593.1:p.Pro1555Ala
XM_017011105.2:c.4633C>G	XP_016866594.1:p.Pro1545Ala
XM_017011106.2:c.4504C>G	XP_016866595.1:p.Pro1502Ala
XM_017011107.2:c.4483C>G	XP_016866596.1:p.Pro1495Ala
XR_002956289.1:n.4778C>G
NM_001363725.2:c.2332C>G	NP_001350654.1:p.Pro778Ala
NM_001371656.1:c.4711C>G	NP_001358585.1:p.Pro1571Ala
NM_001374820.1:c.4711C>G	NP_001361749.1:p.Pro1571Ala
NM_001374828.1:c.4831C>G MANE Select	NP_001361757.1:p.Pro1611Ala
NM_017519.3:c.4672C>G	NP_059989.3:p.Pro1558Ala