Canonical Allele Identifier: CA366242411

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522421A>T (hg19) ; chr6:g.157201287A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201287A>T , CM000668.2:g.157201287A>T	GRCh38
NC_000006.11:g.157522421A>T , CM000668.1:g.157522421A>T	GRCh37
NC_000006.10:g.157564113A>T	NCBI36
NG_032093.1:g.428358A>T
NG_032093.2:g.428358A>T
NG_066624.1:g.430262A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4903A>T	ENSP00000055163.8:p.Asn1635Tyr
ENST00000414678.8:c.4972A>T	ENSP00000412835.3:p.Asn1658Tyr
ENST00000637015.2:c.5191A>T	ENSP00000489729.2:p.Asn1731Tyr
ENST00000346085.10:c.4942A>T	ENSP00000344546.5:p.Asn1648Tyr
ENST00000350026.10:c.4654A>T	ENSP00000055163.7:p.Asn1552Tyr
ENST00000414678.7:c.3220A>T	ENSP00000412835.2:p.Asn1074Tyr
ENST00000635849.1:c.2383A>T	ENSP00000490948.1:p.Asn795Tyr
ENST00000635957.1:c.2014A>T	ENSP00000490385.1:p.Asn672Tyr
ENST00000636227.1:n.3525A>T
ENST00000636254.1:n.982A>T
ENST00000636930.2:c.5062A>T MANE Select	ENSP00000490491.2:p.Asn1688Tyr
ENST00000636940.1:n.3059A>T
ENST00000637015.1:c.2430A>T
ENST00000637568.1:c.2344A>T
ENST00000637741.1:n.1728A>T
ENST00000637810.1:c.2404A>T	ENSP00000489636.1:p.Asn802Tyr
ENST00000637904.1:c.2563A>T	ENSP00000490550.1:p.Asn855Tyr
ENST00000647938.1:c.4693A>T	ENSP00000498155.1:p.Asn1565Tyr
ENST00000346085.9:c.4693A>T	ENSP00000344546.4:p.Asn1565Tyr
ENST00000350026.9:c.4654A>T	ENSP00000055163.7:p.Asn1552Tyr
ENST00000414678.6:c.3220A>T	ENSP00000412835.2:p.Asn1074Tyr
NM_017519.2:c.4654A>T	NP_059989.2:p.Asn1552Tyr
NM_020732.3:c.4693A>T	NP_065783.3:p.Asn1565Tyr
XM_005267069.3:c.4813A>T	XP_005267126.2:p.Asn1605Tyr
XM_011535984.1:c.3892A>T	XP_011534286.1:p.Asn1298Tyr
XM_011535985.1:c.3712A>T	XP_011534287.1:p.Asn1238Tyr
XM_011535986.1:c.3472A>T	XP_011534288.1:p.Asn1158Tyr
XM_011535987.1:c.3091A>T	XP_011534289.1:p.Asn1031Tyr
XM_011535988.1:c.1954A>T	XP_011534290.1:p.Asn652Tyr
NM_001346813.1:c.4813A>T	NP_001333742.1:p.Asn1605Tyr
NM_001363725.1:c.2563A>T	NP_001350654.1:p.Asn855Tyr
XM_011535984.2:c.5023A>T	XP_011534286.2:p.Asn1675Tyr
XM_011535988.3:c.1954A>T	XP_011534290.1:p.Asn652Tyr
XM_017011103.2:c.4924A>T	XP_016866592.1:p.Asn1642Tyr
XM_017011104.1:c.4894A>T	XP_016866593.1:p.Asn1632Tyr
XM_017011105.2:c.4864A>T	XP_016866594.1:p.Asn1622Tyr
XM_017011106.2:c.4735A>T	XP_016866595.1:p.Asn1579Tyr
XM_017011107.2:c.4714A>T	XP_016866596.1:p.Asn1572Tyr
XR_002956289.1:n.5009A>T
NM_001363725.2:c.2563A>T	NP_001350654.1:p.Asn855Tyr
NM_001371656.1:c.4942A>T	NP_001358585.1:p.Asn1648Tyr
NM_001374820.1:c.4942A>T	NP_001361749.1:p.Asn1648Tyr
NM_001374828.1:c.5062A>T MANE Select	NP_001361757.1:p.Asn1688Tyr
NM_017519.3:c.4903A>T	NP_059989.3:p.Asn1635Tyr