Canonical Allele Identifier: CA366242385

Gene: ARID1B

Linked Data

• gnomAD v4: 6-157201275-C-G
• MyVariant Identifiers: chr6:g.157522409C>G (hg19) ; chr6:g.157201275C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201275C>G , CM000668.2:g.157201275C>G	GRCh38
NC_000006.11:g.157522409C>G , CM000668.1:g.157522409C>G	GRCh37
NC_000006.10:g.157564101C>G	NCBI36
NG_032093.1:g.428346C>G
NG_032093.2:g.428346C>G
NG_066624.1:g.430250C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4891C>G	ENSP00000055163.8:p.Arg1631Gly
ENST00000414678.8:c.4960C>G	ENSP00000412835.3:p.Arg1654Gly
ENST00000637015.2:c.5179C>G	ENSP00000489729.2:p.Arg1727Gly
ENST00000346085.10:c.4930C>G	ENSP00000344546.5:p.Arg1644Gly
ENST00000350026.10:c.4642C>G	ENSP00000055163.7:p.Arg1548Gly
ENST00000414678.7:c.3208C>G	ENSP00000412835.2:p.Arg1070Gly
ENST00000635849.1:c.2371C>G	ENSP00000490948.1:p.Arg791Gly
ENST00000635957.1:c.2002C>G	ENSP00000490385.1:p.Arg668Gly
ENST00000636227.1:n.3513C>G
ENST00000636254.1:n.970C>G
ENST00000636930.2:c.5050C>G MANE Select	ENSP00000490491.2:p.Arg1684Gly
ENST00000636940.1:n.3047C>G
ENST00000637015.1:c.2418C>G
ENST00000637568.1:c.2332C>G
ENST00000637741.1:n.1716C>G
ENST00000637810.1:c.2392C>G	ENSP00000489636.1:p.Arg798Gly
ENST00000637904.1:c.2551C>G	ENSP00000490550.1:p.Arg851Gly
ENST00000647938.1:c.4681C>G	ENSP00000498155.1:p.Arg1561Gly
ENST00000346085.9:c.4681C>G	ENSP00000344546.4:p.Arg1561Gly
ENST00000350026.9:c.4642C>G	ENSP00000055163.7:p.Arg1548Gly
ENST00000414678.6:c.3208C>G	ENSP00000412835.2:p.Arg1070Gly
NM_017519.2:c.4642C>G	NP_059989.2:p.Arg1548Gly
NM_020732.3:c.4681C>G	NP_065783.3:p.Arg1561Gly
XM_005267069.3:c.4801C>G	XP_005267126.2:p.Arg1601Gly
XM_011535984.1:c.3880C>G	XP_011534286.1:p.Arg1294Gly
XM_011535985.1:c.3700C>G	XP_011534287.1:p.Arg1234Gly
XM_011535986.1:c.3460C>G	XP_011534288.1:p.Arg1154Gly
XM_011535987.1:c.3079C>G	XP_011534289.1:p.Arg1027Gly
XM_011535988.1:c.1942C>G	XP_011534290.1:p.Arg648Gly
NM_001346813.1:c.4801C>G	NP_001333742.1:p.Arg1601Gly
NM_001363725.1:c.2551C>G	NP_001350654.1:p.Arg851Gly
XM_011535984.2:c.5011C>G	XP_011534286.2:p.Arg1671Gly
XM_011535988.3:c.1942C>G	XP_011534290.1:p.Arg648Gly
XM_017011103.2:c.4912C>G	XP_016866592.1:p.Arg1638Gly
XM_017011104.1:c.4882C>G	XP_016866593.1:p.Arg1628Gly
XM_017011105.2:c.4852C>G	XP_016866594.1:p.Arg1618Gly
XM_017011106.2:c.4723C>G	XP_016866595.1:p.Arg1575Gly
XM_017011107.2:c.4702C>G	XP_016866596.1:p.Arg1568Gly
XR_002956289.1:n.4997C>G
NM_001363725.2:c.2551C>G	NP_001350654.1:p.Arg851Gly
NM_001371656.1:c.4930C>G	NP_001358585.1:p.Arg1644Gly
NM_001374820.1:c.4930C>G	NP_001361749.1:p.Arg1644Gly
NM_001374828.1:c.5050C>G MANE Select	NP_001361757.1:p.Arg1684Gly
NM_017519.3:c.4891C>G	NP_059989.3:p.Arg1631Gly