Canonical Allele Identifier: CA1675522917

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201064C= , CM000668.2:g.157201064C=	GRCh38
NC_000006.11:g.157522198C= , CM000668.1:g.157522198C=	GRCh37
NC_000006.10:g.157563890C=	NCBI36
NG_032093.1:g.428135C=
NG_032093.2:g.428135C=
NG_066624.1:g.430039C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4680C=	ENSP00000055163.8:p.Tyr1560=
ENST00000414678.8:c.4749C=	ENSP00000412835.3:p.Tyr1583=
ENST00000637015.2:c.4968C=	ENSP00000489729.2:p.Tyr1656=
ENST00000346085.10:c.4719C=	ENSP00000344546.5:p.Tyr1573=
ENST00000350026.10:c.4431C=	ENSP00000055163.7:p.Tyr1477=
ENST00000414678.7:c.2997C=	ENSP00000412835.2:p.Tyr999=
ENST00000635849.1:c.2160C=	ENSP00000490948.1:p.Tyr720=
ENST00000635957.1:c.1791C=	ENSP00000490385.1:p.Tyr597=
ENST00000636227.1:n.3302C=
ENST00000636254.1:n.759C=
ENST00000636930.2:c.4839C= MANE Select	ENSP00000490491.2:p.Tyr1613=
ENST00000636940.1:n.2836C=
ENST00000637015.1:c.2207C=
ENST00000637568.1:c.2121C=
ENST00000637741.1:n.1505C=
ENST00000637810.1:c.2181C=	ENSP00000489636.1:p.Tyr727=
ENST00000637904.1:c.2340C=	ENSP00000490550.1:p.Tyr780=
ENST00000647938.1:c.4470C=	ENSP00000498155.1:p.Tyr1490=
ENST00000346085.9:c.4470C=	ENSP00000344546.4:p.Tyr1490=
ENST00000350026.9:c.4431C=	ENSP00000055163.7:p.Tyr1477=
ENST00000414678.6:c.2997C=	ENSP00000412835.2:p.Tyr999=
NM_017519.2:c.4431C=	NP_059989.2:p.Tyr1477=
NM_020732.3:c.4470C=	NP_065783.3:p.Tyr1490=
XM_005267069.3:c.4590C=	XP_005267126.2:p.Tyr1530=
XM_011535984.1:c.3669C=	XP_011534286.1:p.Tyr1223=
XM_011535985.1:c.3489C=	XP_011534287.1:p.Tyr1163=
XM_011535986.1:c.3249C=	XP_011534288.1:p.Tyr1083=
XM_011535987.1:c.2868C=	XP_011534289.1:p.Tyr956=
XM_011535988.1:c.1731C=	XP_011534290.1:p.Tyr577=
NM_001346813.1:c.4590C=	NP_001333742.1:p.Tyr1530=
NM_001363725.1:c.2340C=	NP_001350654.1:p.Tyr780=
XM_011535984.2:c.4800C=	XP_011534286.2:p.Tyr1600=
XM_011535988.3:c.1731C=	XP_011534290.1:p.Tyr577=
XM_017011103.2:c.4701C=	XP_016866592.1:p.Tyr1567=
XM_017011104.1:c.4671C=	XP_016866593.1:p.Tyr1557=
XM_017011105.2:c.4641C=	XP_016866594.1:p.Tyr1547=
XM_017011106.2:c.4512C=	XP_016866595.1:p.Tyr1504=
XM_017011107.2:c.4491C=	XP_016866596.1:p.Tyr1497=
XR_002956289.1:n.4786C=
NM_001363725.2:c.2340C=	NP_001350654.1:p.Tyr780=
NM_001371656.1:c.4719C=	NP_001358585.1:p.Tyr1573=
NM_001374820.1:c.4719C=	NP_001361749.1:p.Tyr1573=
NM_001374828.1:c.4839C= MANE Select	NP_001361757.1:p.Tyr1613=
NM_017519.3:c.4680C=	NP_059989.3:p.Tyr1560=