Canonical Allele Identifier: CA452978136

Gene: ARID1B

Linked Data

• dbSNP Id: rs563086310
• MyVariant Identifiers: chr6:g.157522309C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201175C>A , CM000668.2:g.157201175C>A	GRCh38
NC_000006.11:g.157522309C>A , CM000668.1:g.157522309C>A	GRCh37
NC_000006.10:g.157564001C>A	NCBI36
NG_032093.1:g.428246C>A
NG_032093.2:g.428246C>A
NG_066624.1:g.430150C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4791C>A	ENSP00000055163.8:p.Ala1597=
ENST00000414678.8:c.4860C>A	ENSP00000412835.3:p.Ala1620=
ENST00000637015.2:c.5079C>A	ENSP00000489729.2:p.Ala1693=
ENST00000346085.10:c.4830C>A	ENSP00000344546.5:p.Ala1610=
ENST00000350026.10:c.4542C>A	ENSP00000055163.7:p.Ala1514=
ENST00000414678.7:c.3108C>A	ENSP00000412835.2:p.Ala1036=
ENST00000635849.1:c.2271C>A	ENSP00000490948.1:p.Ala757=
ENST00000635957.1:c.1902C>A	ENSP00000490385.1:p.Ala634=
ENST00000636227.1:n.3413C>A
ENST00000636254.1:n.870C>A
ENST00000636930.2:c.4950C>A MANE Select	ENSP00000490491.2:p.Ala1650=
ENST00000636940.1:n.2947C>A
ENST00000637015.1:c.2318C>A
ENST00000637568.1:c.2232C>A
ENST00000637741.1:n.1616C>A
ENST00000637810.1:c.2292C>A	ENSP00000489636.1:p.Ala764=
ENST00000637904.1:c.2451C>A	ENSP00000490550.1:p.Ala817=
ENST00000647938.1:c.4581C>A	ENSP00000498155.1:p.Ala1527=
ENST00000346085.9:c.4581C>A	ENSP00000344546.4:p.Ala1527=
ENST00000350026.9:c.4542C>A	ENSP00000055163.7:p.Ala1514=
ENST00000414678.6:c.3108C>A	ENSP00000412835.2:p.Ala1036=
NM_017519.2:c.4542C>A	NP_059989.2:p.Ala1514=
NM_020732.3:c.4581C>A	NP_065783.3:p.Ala1527=
XM_005267069.3:c.4701C>A	XP_005267126.2:p.Ala1567=
XM_011535984.1:c.3780C>A	XP_011534286.1:p.Ala1260=
XM_011535985.1:c.3600C>A	XP_011534287.1:p.Ala1200=
XM_011535986.1:c.3360C>A	XP_011534288.1:p.Ala1120=
XM_011535987.1:c.2979C>A	XP_011534289.1:p.Ala993=
XM_011535988.1:c.1842C>A	XP_011534290.1:p.Ala614=
NM_001346813.1:c.4701C>A	NP_001333742.1:p.Ala1567=
NM_001363725.1:c.2451C>A	NP_001350654.1:p.Ala817=
XM_011535984.2:c.4911C>A	XP_011534286.2:p.Ala1637=
XM_011535988.3:c.1842C>A	XP_011534290.1:p.Ala614=
XM_017011103.2:c.4812C>A	XP_016866592.1:p.Ala1604=
XM_017011104.1:c.4782C>A	XP_016866593.1:p.Ala1594=
XM_017011105.2:c.4752C>A	XP_016866594.1:p.Ala1584=
XM_017011106.2:c.4623C>A	XP_016866595.1:p.Ala1541=
XM_017011107.2:c.4602C>A	XP_016866596.1:p.Ala1534=
XR_002956289.1:n.4897C>A
NM_001363725.2:c.2451C>A	NP_001350654.1:p.Ala817=
NM_001371656.1:c.4830C>A	NP_001358585.1:p.Ala1610=
NM_001374820.1:c.4830C>A	NP_001361749.1:p.Ala1610=
NM_001374828.1:c.4950C>A MANE Select	NP_001361757.1:p.Ala1650=
NM_017519.3:c.4791C>A	NP_059989.3:p.Ala1597=