Canonical Allele Identifier: CA366242146

Gene: ARID1B

Linked Data

• dbSNP Id: rs1217807616
• MyVariant Identifiers: chr6:g.157522296T>G (hg19) ; chr6:g.157201162T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201162T>G , CM000668.2:g.157201162T>G	GRCh38
NC_000006.11:g.157522296T>G , CM000668.1:g.157522296T>G	GRCh37
NC_000006.10:g.157563988T>G	NCBI36
NG_032093.1:g.428233T>G
NG_032093.2:g.428233T>G
NG_066624.1:g.430137T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4778T>G	ENSP00000055163.8:p.Met1593Arg
ENST00000414678.8:c.4847T>G	ENSP00000412835.3:p.Met1616Arg
ENST00000637015.2:c.5066T>G	ENSP00000489729.2:p.Met1689Arg
ENST00000346085.10:c.4817T>G	ENSP00000344546.5:p.Met1606Arg
ENST00000350026.10:c.4529T>G	ENSP00000055163.7:p.Met1510Arg
ENST00000414678.7:c.3095T>G	ENSP00000412835.2:p.Met1032Arg
ENST00000635849.1:c.2258T>G	ENSP00000490948.1:p.Met753Arg
ENST00000635957.1:c.1889T>G	ENSP00000490385.1:p.Met630Arg
ENST00000636227.1:n.3400T>G
ENST00000636254.1:n.857T>G
ENST00000636930.2:c.4937T>G MANE Select	ENSP00000490491.2:p.Met1646Arg
ENST00000636940.1:n.2934T>G
ENST00000637015.1:c.2305T>G
ENST00000637568.1:c.2219T>G
ENST00000637741.1:n.1603T>G
ENST00000637810.1:c.2279T>G	ENSP00000489636.1:p.Met760Arg
ENST00000637904.1:c.2438T>G	ENSP00000490550.1:p.Met813Arg
ENST00000647938.1:c.4568T>G	ENSP00000498155.1:p.Met1523Arg
ENST00000346085.9:c.4568T>G	ENSP00000344546.4:p.Met1523Arg
ENST00000350026.9:c.4529T>G	ENSP00000055163.7:p.Met1510Arg
ENST00000414678.6:c.3095T>G	ENSP00000412835.2:p.Met1032Arg
NM_017519.2:c.4529T>G	NP_059989.2:p.Met1510Arg
NM_020732.3:c.4568T>G	NP_065783.3:p.Met1523Arg
XM_005267069.3:c.4688T>G	XP_005267126.2:p.Met1563Arg
XM_011535984.1:c.3767T>G	XP_011534286.1:p.Met1256Arg
XM_011535985.1:c.3587T>G	XP_011534287.1:p.Met1196Arg
XM_011535986.1:c.3347T>G	XP_011534288.1:p.Met1116Arg
XM_011535987.1:c.2966T>G	XP_011534289.1:p.Met989Arg
XM_011535988.1:c.1829T>G	XP_011534290.1:p.Met610Arg
NM_001346813.1:c.4688T>G	NP_001333742.1:p.Met1563Arg
NM_001363725.1:c.2438T>G	NP_001350654.1:p.Met813Arg
XM_011535984.2:c.4898T>G	XP_011534286.2:p.Met1633Arg
XM_011535988.3:c.1829T>G	XP_011534290.1:p.Met610Arg
XM_017011103.2:c.4799T>G	XP_016866592.1:p.Met1600Arg
XM_017011104.1:c.4769T>G	XP_016866593.1:p.Met1590Arg
XM_017011105.2:c.4739T>G	XP_016866594.1:p.Met1580Arg
XM_017011106.2:c.4610T>G	XP_016866595.1:p.Met1537Arg
XM_017011107.2:c.4589T>G	XP_016866596.1:p.Met1530Arg
XR_002956289.1:n.4884T>G
NM_001363725.2:c.2438T>G	NP_001350654.1:p.Met813Arg
NM_001371656.1:c.4817T>G	NP_001358585.1:p.Met1606Arg
NM_001374820.1:c.4817T>G	NP_001361749.1:p.Met1606Arg
NM_001374828.1:c.4937T>G MANE Select	NP_001361757.1:p.Met1646Arg
NM_017519.3:c.4778T>G	NP_059989.3:p.Met1593Arg