Canonical Allele Identifier: CA366241922

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128374486
• MyVariant Identifiers: chr6:g.157522222T>G (hg19) ; chr6:g.157201088T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201088T>G , CM000668.2:g.157201088T>G	GRCh38
NC_000006.11:g.157522222T>G , CM000668.1:g.157522222T>G	GRCh37
NC_000006.10:g.157563914T>G	NCBI36
NG_032093.1:g.428159T>G
NG_032093.2:g.428159T>G
NG_066624.1:g.430063T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4704T>G	ENSP00000055163.8:p.Asp1568Glu
ENST00000414678.8:c.4773T>G	ENSP00000412835.3:p.Asp1591Glu
ENST00000637015.2:c.4992T>G	ENSP00000489729.2:p.Asp1664Glu
ENST00000346085.10:c.4743T>G	ENSP00000344546.5:p.Asp1581Glu
ENST00000350026.10:c.4455T>G	ENSP00000055163.7:p.Asp1485Glu
ENST00000414678.7:c.3021T>G	ENSP00000412835.2:p.Asp1007Glu
ENST00000635849.1:c.2184T>G	ENSP00000490948.1:p.Asp728Glu
ENST00000635957.1:c.1815T>G	ENSP00000490385.1:p.Asp605Glu
ENST00000636227.1:n.3326T>G
ENST00000636254.1:n.783T>G
ENST00000636930.2:c.4863T>G MANE Select	ENSP00000490491.2:p.Asp1621Glu
ENST00000636940.1:n.2860T>G
ENST00000637015.1:c.2231T>G
ENST00000637568.1:c.2145T>G
ENST00000637741.1:n.1529T>G
ENST00000637810.1:c.2205T>G	ENSP00000489636.1:p.Asp735Glu
ENST00000637904.1:c.2364T>G	ENSP00000490550.1:p.Asp788Glu
ENST00000647938.1:c.4494T>G	ENSP00000498155.1:p.Asp1498Glu
ENST00000346085.9:c.4494T>G	ENSP00000344546.4:p.Asp1498Glu
ENST00000350026.9:c.4455T>G	ENSP00000055163.7:p.Asp1485Glu
ENST00000414678.6:c.3021T>G	ENSP00000412835.2:p.Asp1007Glu
NM_017519.2:c.4455T>G	NP_059989.2:p.Asp1485Glu
NM_020732.3:c.4494T>G	NP_065783.3:p.Asp1498Glu
XM_005267069.3:c.4614T>G	XP_005267126.2:p.Asp1538Glu
XM_011535984.1:c.3693T>G	XP_011534286.1:p.Asp1231Glu
XM_011535985.1:c.3513T>G	XP_011534287.1:p.Asp1171Glu
XM_011535986.1:c.3273T>G	XP_011534288.1:p.Asp1091Glu
XM_011535987.1:c.2892T>G	XP_011534289.1:p.Asp964Glu
XM_011535988.1:c.1755T>G	XP_011534290.1:p.Asp585Glu
NM_001346813.1:c.4614T>G	NP_001333742.1:p.Asp1538Glu
NM_001363725.1:c.2364T>G	NP_001350654.1:p.Asp788Glu
XM_011535984.2:c.4824T>G	XP_011534286.2:p.Asp1608Glu
XM_011535988.3:c.1755T>G	XP_011534290.1:p.Asp585Glu
XM_017011103.2:c.4725T>G	XP_016866592.1:p.Asp1575Glu
XM_017011104.1:c.4695T>G	XP_016866593.1:p.Asp1565Glu
XM_017011105.2:c.4665T>G	XP_016866594.1:p.Asp1555Glu
XM_017011106.2:c.4536T>G	XP_016866595.1:p.Asp1512Glu
XM_017011107.2:c.4515T>G	XP_016866596.1:p.Asp1505Glu
XR_002956289.1:n.4810T>G
NM_001363725.2:c.2364T>G	NP_001350654.1:p.Asp788Glu
NM_001371656.1:c.4743T>G	NP_001358585.1:p.Asp1581Glu
NM_001374820.1:c.4743T>G	NP_001361749.1:p.Asp1581Glu
NM_001374828.1:c.4863T>G MANE Select	NP_001361757.1:p.Asp1621Glu
NM_017519.3:c.4704T>G	NP_059989.3:p.Asp1568Glu