Canonical Allele Identifier: CA366242932

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128376572
• MyVariant Identifiers: chr6:g.157522534C>G (hg19) ; chr6:g.157201400C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201400C>G , CM000668.2:g.157201400C>G	GRCh38
NC_000006.11:g.157522534C>G , CM000668.1:g.157522534C>G	GRCh37
NC_000006.10:g.157564226C>G	NCBI36
NG_032093.1:g.428471C>G
NG_032093.2:g.428471C>G
NG_066624.1:g.430375C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.5016C>G	ENSP00000055163.8:p.Ile1672Met
ENST00000414678.8:c.5085C>G	ENSP00000412835.3:p.Ile1695Met
ENST00000637015.2:c.5304C>G	ENSP00000489729.2:p.Ile1768Met
ENST00000346085.10:c.5055C>G	ENSP00000344546.5:p.Ile1685Met
ENST00000350026.10:c.4767C>G	ENSP00000055163.7:p.Ile1589Met
ENST00000414678.7:c.3333C>G	ENSP00000412835.2:p.Ile1111Met
ENST00000635849.1:c.2496C>G	ENSP00000490948.1:p.Ile832Met
ENST00000635957.1:c.2127C>G	ENSP00000490385.1:p.Ile709Met
ENST00000636227.1:n.3638C>G
ENST00000636254.1:n.1095C>G
ENST00000636930.2:c.5175C>G MANE Select	ENSP00000490491.2:p.Ile1725Met
ENST00000636940.1:n.3172C>G
ENST00000637015.1:c.2543C>G
ENST00000637568.1:c.2457C>G
ENST00000637741.1:n.1841C>G
ENST00000637810.1:c.2517C>G	ENSP00000489636.1:p.Ile839Met
ENST00000637904.1:c.2676C>G	ENSP00000490550.1:p.Ile892Met
ENST00000647938.1:c.4806C>G	ENSP00000498155.1:p.Ile1602Met
ENST00000346085.9:c.4806C>G	ENSP00000344546.4:p.Ile1602Met
ENST00000350026.9:c.4767C>G	ENSP00000055163.7:p.Ile1589Met
ENST00000414678.6:c.3333C>G	ENSP00000412835.2:p.Ile1111Met
NM_017519.2:c.4767C>G	NP_059989.2:p.Ile1589Met
NM_020732.3:c.4806C>G	NP_065783.3:p.Ile1602Met
XM_005267069.3:c.4926C>G	XP_005267126.2:p.Ile1642Met
XM_011535984.1:c.4005C>G	XP_011534286.1:p.Ile1335Met
XM_011535985.1:c.3825C>G	XP_011534287.1:p.Ile1275Met
XM_011535986.1:c.3585C>G	XP_011534288.1:p.Ile1195Met
XM_011535987.1:c.3204C>G	XP_011534289.1:p.Ile1068Met
XM_011535988.1:c.2067C>G	XP_011534290.1:p.Ile689Met
NM_001346813.1:c.4926C>G	NP_001333742.1:p.Ile1642Met
NM_001363725.1:c.2676C>G	NP_001350654.1:p.Ile892Met
XM_011535984.2:c.5136C>G	XP_011534286.2:p.Ile1712Met
XM_011535988.3:c.2067C>G	XP_011534290.1:p.Ile689Met
XM_017011103.2:c.5037C>G	XP_016866592.1:p.Ile1679Met
XM_017011104.1:c.5007C>G	XP_016866593.1:p.Ile1669Met
XM_017011105.2:c.4977C>G	XP_016866594.1:p.Ile1659Met
XM_017011106.2:c.4848C>G	XP_016866595.1:p.Ile1616Met
XM_017011107.2:c.4827C>G	XP_016866596.1:p.Ile1609Met
XR_002956289.1:n.5122C>G
NM_001363725.2:c.2676C>G	NP_001350654.1:p.Ile892Met
NM_001371656.1:c.5055C>G	NP_001358585.1:p.Ile1685Met
NM_001374820.1:c.5055C>G	NP_001361749.1:p.Ile1685Met
NM_001374828.1:c.5175C>G MANE Select	NP_001361757.1:p.Ile1725Met
NM_017519.3:c.5016C>G	NP_059989.3:p.Ile1672Met