Canonical Allele Identifier: CA366242011

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522240G>T (hg19) ; chr6:g.157201106G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201106G>T , CM000668.2:g.157201106G>T	GRCh38
NC_000006.11:g.157522240G>T , CM000668.1:g.157522240G>T	GRCh37
NC_000006.10:g.157563932G>T	NCBI36
NG_032093.1:g.428177G>T
NG_032093.2:g.428177G>T
NG_066624.1:g.430081G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4722G>T	ENSP00000055163.8:p.Gln1574His
ENST00000414678.8:c.4791G>T	ENSP00000412835.3:p.Gln1597His
ENST00000637015.2:c.5010G>T	ENSP00000489729.2:p.Gln1670His
ENST00000346085.10:c.4761G>T	ENSP00000344546.5:p.Gln1587His
ENST00000350026.10:c.4473G>T	ENSP00000055163.7:p.Gln1491His
ENST00000414678.7:c.3039G>T	ENSP00000412835.2:p.Gln1013His
ENST00000635849.1:c.2202G>T	ENSP00000490948.1:p.Gln734His
ENST00000635957.1:c.1833G>T	ENSP00000490385.1:p.Gln611His
ENST00000636227.1:n.3344G>T
ENST00000636254.1:n.801G>T
ENST00000636930.2:c.4881G>T MANE Select	ENSP00000490491.2:p.Gln1627His
ENST00000636940.1:n.2878G>T
ENST00000637015.1:c.2249G>T
ENST00000637568.1:c.2163G>T
ENST00000637741.1:n.1547G>T
ENST00000637810.1:c.2223G>T	ENSP00000489636.1:p.Gln741His
ENST00000637904.1:c.2382G>T	ENSP00000490550.1:p.Gln794His
ENST00000647938.1:c.4512G>T	ENSP00000498155.1:p.Gln1504His
ENST00000346085.9:c.4512G>T	ENSP00000344546.4:p.Gln1504His
ENST00000350026.9:c.4473G>T	ENSP00000055163.7:p.Gln1491His
ENST00000414678.6:c.3039G>T	ENSP00000412835.2:p.Gln1013His
NM_017519.2:c.4473G>T	NP_059989.2:p.Gln1491His
NM_020732.3:c.4512G>T	NP_065783.3:p.Gln1504His
XM_005267069.3:c.4632G>T	XP_005267126.2:p.Gln1544His
XM_011535984.1:c.3711G>T	XP_011534286.1:p.Gln1237His
XM_011535985.1:c.3531G>T	XP_011534287.1:p.Gln1177His
XM_011535986.1:c.3291G>T	XP_011534288.1:p.Gln1097His
XM_011535987.1:c.2910G>T	XP_011534289.1:p.Gln970His
XM_011535988.1:c.1773G>T	XP_011534290.1:p.Gln591His
NM_001346813.1:c.4632G>T	NP_001333742.1:p.Gln1544His
NM_001363725.1:c.2382G>T	NP_001350654.1:p.Gln794His
XM_011535984.2:c.4842G>T	XP_011534286.2:p.Gln1614His
XM_011535988.3:c.1773G>T	XP_011534290.1:p.Gln591His
XM_017011103.2:c.4743G>T	XP_016866592.1:p.Gln1581His
XM_017011104.1:c.4713G>T	XP_016866593.1:p.Gln1571His
XM_017011105.2:c.4683G>T	XP_016866594.1:p.Gln1561His
XM_017011106.2:c.4554G>T	XP_016866595.1:p.Gln1518His
XM_017011107.2:c.4533G>T	XP_016866596.1:p.Gln1511His
XR_002956289.1:n.4828G>T
NM_001363725.2:c.2382G>T	NP_001350654.1:p.Gln794His
NM_001371656.1:c.4761G>T	NP_001358585.1:p.Gln1587His
NM_001374820.1:c.4761G>T	NP_001361749.1:p.Gln1587His
NM_001374828.1:c.4881G>T MANE Select	NP_001361757.1:p.Gln1627His
NM_017519.3:c.4722G>T	NP_059989.3:p.Gln1574His