Canonical Allele Identifier: CA452978050

Gene: ARID1B

Linked Data

• dbSNP Id: rs1433067280
• gnomAD v2: 6-157522240-G-A
• MyVariant Identifiers: chr6:g.157522240G>A (hg19) ; chr6:g.157201106G>A (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4722G>A	ENSP00000055163.8:p.Gln1574=
ENST00000414678.8:c.4791G>A	ENSP00000412835.3:p.Gln1597=
ENST00000637015.2:c.5010G>A	ENSP00000489729.2:p.Gln1670=
ENST00000346085.10:c.4761G>A	ENSP00000344546.5:p.Gln1587=
ENST00000350026.10:c.4473G>A	ENSP00000055163.7:p.Gln1491=
ENST00000414678.7:c.3039G>A	ENSP00000412835.2:p.Gln1013=
ENST00000635849.1:c.2202G>A	ENSP00000490948.1:p.Gln734=
ENST00000635957.1:c.1833G>A	ENSP00000490385.1:p.Gln611=
ENST00000636227.1:n.3344G>A
ENST00000636254.1:n.801G>A
ENST00000636930.2:c.4881G>A MANE Select	ENSP00000490491.2:p.Gln1627=
ENST00000636940.1:n.2878G>A
ENST00000637015.1:c.2249G>A
ENST00000637568.1:c.2163G>A
ENST00000637741.1:n.1547G>A
ENST00000637810.1:c.2223G>A	ENSP00000489636.1:p.Gln741=
ENST00000637904.1:c.2382G>A	ENSP00000490550.1:p.Gln794=
ENST00000647938.1:c.4512G>A	ENSP00000498155.1:p.Gln1504=
ENST00000346085.9:c.4512G>A	ENSP00000344546.4:p.Gln1504=
ENST00000350026.9:c.4473G>A	ENSP00000055163.7:p.Gln1491=
ENST00000414678.6:c.3039G>A	ENSP00000412835.2:p.Gln1013=
NM_017519.2:c.4473G>A	NP_059989.2:p.Gln1491=
NM_020732.3:c.4512G>A	NP_065783.3:p.Gln1504=
XM_005267069.3:c.4632G>A	XP_005267126.2:p.Gln1544=
XM_011535984.1:c.3711G>A	XP_011534286.1:p.Gln1237=
XM_011535985.1:c.3531G>A	XP_011534287.1:p.Gln1177=
XM_011535986.1:c.3291G>A	XP_011534288.1:p.Gln1097=
XM_011535987.1:c.2910G>A	XP_011534289.1:p.Gln970=
XM_011535988.1:c.1773G>A	XP_011534290.1:p.Gln591=
NM_001346813.1:c.4632G>A	NP_001333742.1:p.Gln1544=
NM_001363725.1:c.2382G>A	NP_001350654.1:p.Gln794=
XM_011535984.2:c.4842G>A	XP_011534286.2:p.Gln1614=
XM_011535988.3:c.1773G>A	XP_011534290.1:p.Gln591=
XM_017011103.2:c.4743G>A	XP_016866592.1:p.Gln1581=
XM_017011104.1:c.4713G>A	XP_016866593.1:p.Gln1571=
XM_017011105.2:c.4683G>A	XP_016866594.1:p.Gln1561=
XM_017011106.2:c.4554G>A	XP_016866595.1:p.Gln1518=
XM_017011107.2:c.4533G>A	XP_016866596.1:p.Gln1511=
XR_002956289.1:n.4828G>A
NM_001363725.2:c.2382G>A	NP_001350654.1:p.Gln794=
NM_001371656.1:c.4761G>A	NP_001358585.1:p.Gln1587=
NM_001374820.1:c.4761G>A	NP_001361749.1:p.Gln1587=
NM_001374828.1:c.4881G>A MANE Select	NP_001361757.1:p.Gln1627=
NM_017519.3:c.4722G>A	NP_059989.3:p.Gln1574=