Canonical Allele Identifier: CA366234052

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510804G>T (hg19) ; chr6:g.157189670G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189670G>T , CM000668.2:g.157189670G>T	GRCh38
NC_000006.11:g.157510804G>T , CM000668.1:g.157510804G>T	GRCh37
NC_000006.10:g.157552496G>T	NCBI36
NG_032093.1:g.416741G>T
NG_032093.2:g.416741G>T
NG_066624.1:g.418645G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3789G>T	ENSP00000055163.8:p.Gln1263His
ENST00000414678.8:c.3858G>T	ENSP00000412835.3:p.Gln1286His
ENST00000637015.2:c.4077G>T	ENSP00000489729.2:p.Gln1359His
ENST00000346085.10:c.3828G>T	ENSP00000344546.5:p.Gln1276His
ENST00000350026.10:c.3540G>T	ENSP00000055163.7:p.Gln1180His
ENST00000414678.7:c.2106G>T	ENSP00000412835.2:p.Gln702His
ENST00000635849.1:c.1269G>T	ENSP00000490948.1:p.Gln423His
ENST00000635957.1:c.903G>T	ENSP00000490385.1:p.Gln301His
ENST00000636930.2:c.3948G>T MANE Select	ENSP00000490491.2:p.Gln1316His
ENST00000636940.1:n.1945G>T
ENST00000637015.1:c.1316G>T
ENST00000637568.1:c.1230G>T
ENST00000637741.1:n.614G>T
ENST00000637810.1:c.1290G>T	ENSP00000489636.1:p.Gln430His
ENST00000637904.1:c.1449G>T	ENSP00000490550.1:p.Gln483His
ENST00000647938.1:c.3579G>T	ENSP00000498155.1:p.Gln1193His
ENST00000346085.9:c.3579G>T	ENSP00000344546.4:p.Gln1193His
ENST00000350026.9:c.3540G>T	ENSP00000055163.7:p.Gln1180His
ENST00000414678.6:c.2106G>T	ENSP00000412835.2:p.Gln702His
NM_017519.2:c.3540G>T	NP_059989.2:p.Gln1180His
NM_020732.3:c.3579G>T	NP_065783.3:p.Gln1193His
XM_005267069.3:c.3699G>T	XP_005267126.2:p.Gln1233His
XM_011535984.1:c.2778G>T	XP_011534286.1:p.Gln926His
XM_011535985.1:c.2598G>T	XP_011534287.1:p.Gln866His
XM_011535986.1:c.2358G>T	XP_011534288.1:p.Gln786His
XM_011535987.1:c.1977G>T	XP_011534289.1:p.Gln659His
XM_011535988.1:c.840G>T	XP_011534290.1:p.Gln280His
NM_001346813.1:c.3699G>T	NP_001333742.1:p.Gln1233His
NM_001363725.1:c.1449G>T	NP_001350654.1:p.Gln483His
XM_011535984.2:c.3909G>T	XP_011534286.2:p.Gln1303His
XM_011535988.3:c.840G>T	XP_011534290.1:p.Gln280His
XM_017011103.2:c.3810G>T	XP_016866592.1:p.Gln1270His
XM_017011104.1:c.3780G>T	XP_016866593.1:p.Gln1260His
XM_017011105.2:c.3750G>T	XP_016866594.1:p.Gln1250His
XM_017011106.2:c.3621G>T	XP_016866595.1:p.Gln1207His
XM_017011107.2:c.3600G>T	XP_016866596.1:p.Gln1200His
XR_002956289.1:n.3992G>T
NM_001363725.2:c.1449G>T	NP_001350654.1:p.Gln483His
NM_001371656.1:c.3828G>T	NP_001358585.1:p.Gln1276His
NM_001374820.1:c.3828G>T	NP_001361749.1:p.Gln1276His
NM_001374828.1:c.3948G>T MANE Select	NP_001361757.1:p.Gln1316His
NM_017519.3:c.3789G>T	NP_059989.3:p.Gln1263His