Canonical Allele Identifier: CA366230333

Gene: ARID1B

Linked Data

• dbSNP Id: rs1554231836
• MyVariant Identifiers: chr6:g.157505449C>G (hg19) ; chr6:g.157184315C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157184315C>G , CM000668.2:g.157184315C>G	GRCh38
NC_000006.11:g.157505449C>G , CM000668.1:g.157505449C>G	GRCh37
NC_000006.10:g.157547141C>G	NCBI36
NG_032093.1:g.411386C>G
NG_032093.2:g.411386C>G
NG_066624.1:g.413290C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3640C>G	ENSP00000055163.8:p.Gln1214Glu
ENST00000414678.8:c.3709C>G	ENSP00000412835.3:p.Gln1237Glu
ENST00000637015.2:c.3928C>G	ENSP00000489729.2:p.Gln1310Glu
ENST00000319584.11:c.1813C>G	ENSP00000313006.7:p.Gln605Glu
ENST00000346085.10:c.3679C>G	ENSP00000344546.5:p.Gln1227Glu
ENST00000350026.10:c.3391C>G	ENSP00000055163.7:p.Gln1131Glu
ENST00000414678.7:c.1957C>G	ENSP00000412835.2:p.Gln653Glu
ENST00000635849.1:c.1120C>G	ENSP00000490948.1:p.Gln374Glu
ENST00000635957.1:c.754C>G	ENSP00000490385.1:p.Gln252Glu
ENST00000636930.2:c.3799C>G MANE Select	ENSP00000490491.2:p.Gln1267Glu
ENST00000636940.1:n.1796C>G
ENST00000637015.1:c.1167C>G
ENST00000637568.1:c.1081C>G
ENST00000637741.1:n.465C>G
ENST00000637810.1:c.1141C>G	ENSP00000489636.1:p.Gln381Glu
ENST00000637904.1:c.1300C>G	ENSP00000490550.1:p.Gln434Glu
ENST00000647938.1:c.3430C>G	ENSP00000498155.1:p.Gln1144Glu
ENST00000319584.10:c.1816C>G	ENSP00000313006.6:p.Gln606Glu
ENST00000346085.9:c.3430C>G	ENSP00000344546.4:p.Gln1144Glu
ENST00000350026.9:c.3391C>G	ENSP00000055163.7:p.Gln1131Glu
ENST00000400790.3:c.592C>G	ENSP00000383596.3:p.Gln198Glu
ENST00000414678.6:c.1957C>G	ENSP00000412835.2:p.Gln653Glu
NM_017519.2:c.3391C>G	NP_059989.2:p.Gln1131Glu
NM_020732.3:c.3430C>G	NP_065783.3:p.Gln1144Glu
XM_005267069.3:c.3550C>G	XP_005267126.2:p.Gln1184Glu
XM_011535984.1:c.2629C>G	XP_011534286.1:p.Gln877Glu
XM_011535985.1:c.2449C>G	XP_011534287.1:p.Gln817Glu
XM_011535986.1:c.2209C>G	XP_011534288.1:p.Gln737Glu
XM_011535987.1:c.1828C>G	XP_011534289.1:p.Gln610Glu
XM_011535988.1:c.691C>G	XP_011534290.1:p.Gln231Glu
NM_001346813.1:c.3550C>G	NP_001333742.1:p.Gln1184Glu
NM_001363725.1:c.1300C>G	NP_001350654.1:p.Gln434Glu
XM_011535984.2:c.3760C>G	XP_011534286.2:p.Gln1254Glu
XM_011535988.3:c.691C>G	XP_011534290.1:p.Gln231Glu
XM_017011103.2:c.3661C>G	XP_016866592.1:p.Gln1221Glu
XM_017011104.1:c.3631C>G	XP_016866593.1:p.Gln1211Glu
XM_017011105.2:c.3601C>G	XP_016866594.1:p.Gln1201Glu
XM_017011106.2:c.3472C>G	XP_016866595.1:p.Gln1158Glu
XM_017011107.2:c.3451C>G	XP_016866596.1:p.Gln1151Glu
XR_002956289.1:n.3843C>G
NM_001363725.2:c.1300C>G	NP_001350654.1:p.Gln434Glu
NM_001371656.1:c.3679C>G	NP_001358585.1:p.Gln1227Glu
NM_001374820.1:c.3679C>G	NP_001361749.1:p.Gln1227Glu
NM_001374828.1:c.3799C>G MANE Select	NP_001361757.1:p.Gln1267Glu
NM_017519.3:c.3640C>G	NP_059989.3:p.Gln1214Glu