Canonical Allele Identifier: CA1675523552

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201398A= , CM000668.2:g.157201398A=	GRCh38
NC_000006.11:g.157522532A= , CM000668.1:g.157522532A=	GRCh37
NC_000006.10:g.157564224A=	NCBI36
NG_032093.1:g.428469A=
NG_032093.2:g.428469A=
NG_066624.1:g.430373A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.5014A=	ENSP00000055163.8:p.Ile1672=
ENST00000414678.8:c.5083A=	ENSP00000412835.3:p.Ile1695=
ENST00000637015.2:c.5302A=	ENSP00000489729.2:p.Ile1768=
ENST00000346085.10:c.5053A=	ENSP00000344546.5:p.Ile1685=
ENST00000350026.10:c.4765A=	ENSP00000055163.7:p.Ile1589=
ENST00000414678.7:c.3331A=	ENSP00000412835.2:p.Ile1111=
ENST00000635849.1:c.2494A=	ENSP00000490948.1:p.Ile832=
ENST00000635957.1:c.2125A=	ENSP00000490385.1:p.Ile709=
ENST00000636227.1:n.3636A=
ENST00000636254.1:n.1093A=
ENST00000636930.2:c.5173A= MANE Select	ENSP00000490491.2:p.Ile1725=
ENST00000636940.1:n.3170A=
ENST00000637015.1:c.2541A=
ENST00000637568.1:c.2455A=
ENST00000637741.1:n.1839A=
ENST00000637810.1:c.2515A=	ENSP00000489636.1:p.Ile839=
ENST00000637904.1:c.2674A=	ENSP00000490550.1:p.Ile892=
ENST00000647938.1:c.4804A=	ENSP00000498155.1:p.Ile1602=
ENST00000346085.9:c.4804A=	ENSP00000344546.4:p.Ile1602=
ENST00000350026.9:c.4765A=	ENSP00000055163.7:p.Ile1589=
ENST00000414678.6:c.3331A=	ENSP00000412835.2:p.Ile1111=
NM_017519.2:c.4765A=	NP_059989.2:p.Ile1589=
NM_020732.3:c.4804A=	NP_065783.3:p.Ile1602=
XM_005267069.3:c.4924A=	XP_005267126.2:p.Ile1642=
XM_011535984.1:c.4003A=	XP_011534286.1:p.Ile1335=
XM_011535985.1:c.3823A=	XP_011534287.1:p.Ile1275=
XM_011535986.1:c.3583A=	XP_011534288.1:p.Ile1195=
XM_011535987.1:c.3202A=	XP_011534289.1:p.Ile1068=
XM_011535988.1:c.2065A=	XP_011534290.1:p.Ile689=
NM_001346813.1:c.4924A=	NP_001333742.1:p.Ile1642=
NM_001363725.1:c.2674A=	NP_001350654.1:p.Ile892=
XM_011535984.2:c.5134A=	XP_011534286.2:p.Ile1712=
XM_011535988.3:c.2065A=	XP_011534290.1:p.Ile689=
XM_017011103.2:c.5035A=	XP_016866592.1:p.Ile1679=
XM_017011104.1:c.5005A=	XP_016866593.1:p.Ile1669=
XM_017011105.2:c.4975A=	XP_016866594.1:p.Ile1659=
XM_017011106.2:c.4846A=	XP_016866595.1:p.Ile1616=
XM_017011107.2:c.4825A=	XP_016866596.1:p.Ile1609=
XR_002956289.1:n.5120A=
NM_001363725.2:c.2674A=	NP_001350654.1:p.Ile892=
NM_001371656.1:c.5053A=	NP_001358585.1:p.Ile1685=
NM_001374820.1:c.5053A=	NP_001361749.1:p.Ile1685=
NM_001374828.1:c.5173A= MANE Select	NP_001361757.1:p.Ile1725=
NM_017519.3:c.5014A=	NP_059989.3:p.Ile1672=