Canonical Allele Identifier: CA366241997

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522235G>T (hg19) ; chr6:g.157201101G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201101G>T , CM000668.2:g.157201101G>T	GRCh38
NC_000006.11:g.157522235G>T , CM000668.1:g.157522235G>T	GRCh37
NC_000006.10:g.157563927G>T	NCBI36
NG_032093.1:g.428172G>T
NG_032093.2:g.428172G>T
NG_066624.1:g.430076G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4717G>T	ENSP00000055163.8:p.Asp1573Tyr
ENST00000414678.8:c.4786G>T	ENSP00000412835.3:p.Asp1596Tyr
ENST00000637015.2:c.5005G>T	ENSP00000489729.2:p.Asp1669Tyr
ENST00000346085.10:c.4756G>T	ENSP00000344546.5:p.Asp1586Tyr
ENST00000350026.10:c.4468G>T	ENSP00000055163.7:p.Asp1490Tyr
ENST00000414678.7:c.3034G>T	ENSP00000412835.2:p.Asp1012Tyr
ENST00000635849.1:c.2197G>T	ENSP00000490948.1:p.Asp733Tyr
ENST00000635957.1:c.1828G>T	ENSP00000490385.1:p.Asp610Tyr
ENST00000636227.1:n.3339G>T
ENST00000636254.1:n.796G>T
ENST00000636930.2:c.4876G>T MANE Select	ENSP00000490491.2:p.Asp1626Tyr
ENST00000636940.1:n.2873G>T
ENST00000637015.1:c.2244G>T
ENST00000637568.1:c.2158G>T
ENST00000637741.1:n.1542G>T
ENST00000637810.1:c.2218G>T	ENSP00000489636.1:p.Asp740Tyr
ENST00000637904.1:c.2377G>T	ENSP00000490550.1:p.Asp793Tyr
ENST00000647938.1:c.4507G>T	ENSP00000498155.1:p.Asp1503Tyr
ENST00000346085.9:c.4507G>T	ENSP00000344546.4:p.Asp1503Tyr
ENST00000350026.9:c.4468G>T	ENSP00000055163.7:p.Asp1490Tyr
ENST00000414678.6:c.3034G>T	ENSP00000412835.2:p.Asp1012Tyr
NM_017519.2:c.4468G>T	NP_059989.2:p.Asp1490Tyr
NM_020732.3:c.4507G>T	NP_065783.3:p.Asp1503Tyr
XM_005267069.3:c.4627G>T	XP_005267126.2:p.Asp1543Tyr
XM_011535984.1:c.3706G>T	XP_011534286.1:p.Asp1236Tyr
XM_011535985.1:c.3526G>T	XP_011534287.1:p.Asp1176Tyr
XM_011535986.1:c.3286G>T	XP_011534288.1:p.Asp1096Tyr
XM_011535987.1:c.2905G>T	XP_011534289.1:p.Asp969Tyr
XM_011535988.1:c.1768G>T	XP_011534290.1:p.Asp590Tyr
NM_001346813.1:c.4627G>T	NP_001333742.1:p.Asp1543Tyr
NM_001363725.1:c.2377G>T	NP_001350654.1:p.Asp793Tyr
XM_011535984.2:c.4837G>T	XP_011534286.2:p.Asp1613Tyr
XM_011535988.3:c.1768G>T	XP_011534290.1:p.Asp590Tyr
XM_017011103.2:c.4738G>T	XP_016866592.1:p.Asp1580Tyr
XM_017011104.1:c.4708G>T	XP_016866593.1:p.Asp1570Tyr
XM_017011105.2:c.4678G>T	XP_016866594.1:p.Asp1560Tyr
XM_017011106.2:c.4549G>T	XP_016866595.1:p.Asp1517Tyr
XM_017011107.2:c.4528G>T	XP_016866596.1:p.Asp1510Tyr
XR_002956289.1:n.4823G>T
NM_001363725.2:c.2377G>T	NP_001350654.1:p.Asp793Tyr
NM_001371656.1:c.4756G>T	NP_001358585.1:p.Asp1586Tyr
NM_001374820.1:c.4756G>T	NP_001361749.1:p.Asp1586Tyr
NM_001374828.1:c.4876G>T MANE Select	NP_001361757.1:p.Asp1626Tyr
NM_017519.3:c.4717G>T	NP_059989.3:p.Asp1573Tyr