Canonical Allele Identifier: CA366239784

Gene: ARID1B

Linked Data

• dbSNP Id: rs1346388806
• MyVariant Identifiers: chr6:g.157520007G>C (hg19) ; chr6:g.157198873G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157198873G>C , CM000668.2:g.157198873G>C	GRCh38
NC_000006.11:g.157520007G>C , CM000668.1:g.157520007G>C	GRCh37
NC_000006.10:g.157561699G>C	NCBI36
NG_032093.1:g.425944G>C
NG_032093.2:g.425944G>C
NG_066624.1:g.427848G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4286G>C	ENSP00000055163.8:p.Gly1429Ala
ENST00000414678.8:c.4355G>C	ENSP00000412835.3:p.Gly1452Ala
ENST00000637015.2:c.4574G>C	ENSP00000489729.2:p.Gly1525Ala
ENST00000346085.10:c.4325G>C	ENSP00000344546.5:p.Gly1442Ala
ENST00000350026.10:c.4037G>C	ENSP00000055163.7:p.Gly1346Ala
ENST00000414678.7:c.2603G>C	ENSP00000412835.2:p.Gly868Ala
ENST00000635849.1:c.1766G>C	ENSP00000490948.1:p.Gly589Ala
ENST00000635957.1:c.1397G>C	ENSP00000490385.1:p.Gly466Ala
ENST00000636227.1:n.2908G>C
ENST00000636254.1:n.365G>C
ENST00000636930.2:c.4445G>C MANE Select	ENSP00000490491.2:p.Gly1482Ala
ENST00000636940.1:n.2442G>C
ENST00000637015.1:c.1813G>C
ENST00000637568.1:c.1727G>C
ENST00000637741.1:n.1111G>C
ENST00000637810.1:c.1787G>C	ENSP00000489636.1:p.Gly596Ala
ENST00000637904.1:c.1946G>C	ENSP00000490550.1:p.Gly649Ala
ENST00000647938.1:c.4076G>C	ENSP00000498155.1:p.Gly1359Ala
ENST00000346085.9:c.4076G>C	ENSP00000344546.4:p.Gly1359Ala
ENST00000350026.9:c.4037G>C	ENSP00000055163.7:p.Gly1346Ala
ENST00000414678.6:c.2603G>C	ENSP00000412835.2:p.Gly868Ala
NM_017519.2:c.4037G>C	NP_059989.2:p.Gly1346Ala
NM_020732.3:c.4076G>C	NP_065783.3:p.Gly1359Ala
XM_005267069.3:c.4196G>C	XP_005267126.2:p.Gly1399Ala
XM_011535984.1:c.3275G>C	XP_011534286.1:p.Gly1092Ala
XM_011535985.1:c.3095G>C	XP_011534287.1:p.Gly1032Ala
XM_011535986.1:c.2855G>C	XP_011534288.1:p.Gly952Ala
XM_011535987.1:c.2474G>C	XP_011534289.1:p.Gly825Ala
XM_011535988.1:c.1337G>C	XP_011534290.1:p.Gly446Ala
NM_001346813.1:c.4196G>C	NP_001333742.1:p.Gly1399Ala
NM_001363725.1:c.1946G>C	NP_001350654.1:p.Gly649Ala
XM_011535984.2:c.4406G>C	XP_011534286.2:p.Gly1469Ala
XM_011535988.3:c.1337G>C	XP_011534290.1:p.Gly446Ala
XM_017011103.2:c.4307G>C	XP_016866592.1:p.Gly1436Ala
XM_017011104.1:c.4277G>C	XP_016866593.1:p.Gly1426Ala
XM_017011105.2:c.4247G>C	XP_016866594.1:p.Gly1416Ala
XM_017011106.2:c.4118G>C	XP_016866595.1:p.Gly1373Ala
XM_017011107.2:c.4097G>C	XP_016866596.1:p.Gly1366Ala
XR_002956289.1:n.4427-1832G>C
NM_001363725.2:c.1946G>C	NP_001350654.1:p.Gly649Ala
NM_001371656.1:c.4325G>C	NP_001358585.1:p.Gly1442Ala
NM_001374820.1:c.4325G>C	NP_001361749.1:p.Gly1442Ala
NM_001374828.1:c.4445G>C MANE Select	NP_001361757.1:p.Gly1482Ala
NM_017519.3:c.4286G>C	NP_059989.3:p.Gly1429Ala