Canonical Allele Identifier: CA1675523518

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201378C= , CM000668.2:g.157201378C=	GRCh38
NC_000006.11:g.157522512C= , CM000668.1:g.157522512C=	GRCh37
NC_000006.10:g.157564204C=	NCBI36
NG_032093.1:g.428449C=
NG_032093.2:g.428449C=
NG_066624.1:g.430353C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4994C=	ENSP00000055163.8:p.Pro1665=
ENST00000414678.8:c.5063C=	ENSP00000412835.3:p.Pro1688=
ENST00000637015.2:c.5282C=	ENSP00000489729.2:p.Pro1761=
ENST00000346085.10:c.5033C=	ENSP00000344546.5:p.Pro1678=
ENST00000350026.10:c.4745C=	ENSP00000055163.7:p.Pro1582=
ENST00000414678.7:c.3311C=	ENSP00000412835.2:p.Pro1104=
ENST00000635849.1:c.2474C=	ENSP00000490948.1:p.Pro825=
ENST00000635957.1:c.2105C=	ENSP00000490385.1:p.Pro702=
ENST00000636227.1:n.3616C=
ENST00000636254.1:n.1073C=
ENST00000636930.2:c.5153C= MANE Select	ENSP00000490491.2:p.Pro1718=
ENST00000636940.1:n.3150C=
ENST00000637015.1:c.2521C=
ENST00000637568.1:c.2435C=
ENST00000637741.1:n.1819C=
ENST00000637810.1:c.2495C=	ENSP00000489636.1:p.Pro832=
ENST00000637904.1:c.2654C=	ENSP00000490550.1:p.Pro885=
ENST00000647938.1:c.4784C=	ENSP00000498155.1:p.Pro1595=
ENST00000346085.9:c.4784C=	ENSP00000344546.4:p.Pro1595=
ENST00000350026.9:c.4745C=	ENSP00000055163.7:p.Pro1582=
ENST00000414678.6:c.3311C=	ENSP00000412835.2:p.Pro1104=
NM_017519.2:c.4745C=	NP_059989.2:p.Pro1582=
NM_020732.3:c.4784C=	NP_065783.3:p.Pro1595=
XM_005267069.3:c.4904C=	XP_005267126.2:p.Pro1635=
XM_011535984.1:c.3983C=	XP_011534286.1:p.Pro1328=
XM_011535985.1:c.3803C=	XP_011534287.1:p.Pro1268=
XM_011535986.1:c.3563C=	XP_011534288.1:p.Pro1188=
XM_011535987.1:c.3182C=	XP_011534289.1:p.Pro1061=
XM_011535988.1:c.2045C=	XP_011534290.1:p.Pro682=
NM_001346813.1:c.4904C=	NP_001333742.1:p.Pro1635=
NM_001363725.1:c.2654C=	NP_001350654.1:p.Pro885=
XM_011535984.2:c.5114C=	XP_011534286.2:p.Pro1705=
XM_011535988.3:c.2045C=	XP_011534290.1:p.Pro682=
XM_017011103.2:c.5015C=	XP_016866592.1:p.Pro1672=
XM_017011104.1:c.4985C=	XP_016866593.1:p.Pro1662=
XM_017011105.2:c.4955C=	XP_016866594.1:p.Pro1652=
XM_017011106.2:c.4826C=	XP_016866595.1:p.Pro1609=
XM_017011107.2:c.4805C=	XP_016866596.1:p.Pro1602=
XR_002956289.1:n.5100C=
NM_001363725.2:c.2654C=	NP_001350654.1:p.Pro885=
NM_001371656.1:c.5033C=	NP_001358585.1:p.Pro1678=
NM_001374820.1:c.5033C=	NP_001361749.1:p.Pro1678=
NM_001374828.1:c.5153C= MANE Select	NP_001361757.1:p.Pro1718=
NM_017519.3:c.4994C=	NP_059989.3:p.Pro1665=