Canonical Allele Identifier: CA1675523072

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201160T= , CM000668.2:g.157201160T=	GRCh38
NC_000006.11:g.157522294T= , CM000668.1:g.157522294T=	GRCh37
NC_000006.10:g.157563986T=	NCBI36
NG_032093.1:g.428231T=
NG_032093.2:g.428231T=
NG_066624.1:g.430135T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4776T=	ENSP00000055163.8:p.Tyr1592=
ENST00000414678.8:c.4845T=	ENSP00000412835.3:p.Tyr1615=
ENST00000637015.2:c.5064T=	ENSP00000489729.2:p.Tyr1688=
ENST00000346085.10:c.4815T=	ENSP00000344546.5:p.Tyr1605=
ENST00000350026.10:c.4527T=	ENSP00000055163.7:p.Tyr1509=
ENST00000414678.7:c.3093T=	ENSP00000412835.2:p.Tyr1031=
ENST00000635849.1:c.2256T=	ENSP00000490948.1:p.Tyr752=
ENST00000635957.1:c.1887T=	ENSP00000490385.1:p.Tyr629=
ENST00000636227.1:n.3398T=
ENST00000636254.1:n.855T=
ENST00000636930.2:c.4935T= MANE Select	ENSP00000490491.2:p.Tyr1645=
ENST00000636940.1:n.2932T=
ENST00000637015.1:c.2303T=
ENST00000637568.1:c.2217T=
ENST00000637741.1:n.1601T=
ENST00000637810.1:c.2277T=	ENSP00000489636.1:p.Tyr759=
ENST00000637904.1:c.2436T=	ENSP00000490550.1:p.Tyr812=
ENST00000647938.1:c.4566T=	ENSP00000498155.1:p.Tyr1522=
ENST00000346085.9:c.4566T=	ENSP00000344546.4:p.Tyr1522=
ENST00000350026.9:c.4527T=	ENSP00000055163.7:p.Tyr1509=
ENST00000414678.6:c.3093T=	ENSP00000412835.2:p.Tyr1031=
NM_017519.2:c.4527T=	NP_059989.2:p.Tyr1509=
NM_020732.3:c.4566T=	NP_065783.3:p.Tyr1522=
XM_005267069.3:c.4686T=	XP_005267126.2:p.Tyr1562=
XM_011535984.1:c.3765T=	XP_011534286.1:p.Tyr1255=
XM_011535985.1:c.3585T=	XP_011534287.1:p.Tyr1195=
XM_011535986.1:c.3345T=	XP_011534288.1:p.Tyr1115=
XM_011535987.1:c.2964T=	XP_011534289.1:p.Tyr988=
XM_011535988.1:c.1827T=	XP_011534290.1:p.Tyr609=
NM_001346813.1:c.4686T=	NP_001333742.1:p.Tyr1562=
NM_001363725.1:c.2436T=	NP_001350654.1:p.Tyr812=
XM_011535984.2:c.4896T=	XP_011534286.2:p.Tyr1632=
XM_011535988.3:c.1827T=	XP_011534290.1:p.Tyr609=
XM_017011103.2:c.4797T=	XP_016866592.1:p.Tyr1599=
XM_017011104.1:c.4767T=	XP_016866593.1:p.Tyr1589=
XM_017011105.2:c.4737T=	XP_016866594.1:p.Tyr1579=
XM_017011106.2:c.4608T=	XP_016866595.1:p.Tyr1536=
XM_017011107.2:c.4587T=	XP_016866596.1:p.Tyr1529=
XR_002956289.1:n.4882T=
NM_001363725.2:c.2436T=	NP_001350654.1:p.Tyr812=
NM_001371656.1:c.4815T=	NP_001358585.1:p.Tyr1605=
NM_001374820.1:c.4815T=	NP_001361749.1:p.Tyr1605=
NM_001374828.1:c.4935T= MANE Select	NP_001361757.1:p.Tyr1645=
NM_017519.3:c.4776T=	NP_059989.3:p.Tyr1592=