Canonical Allele Identifier: CA452978157

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522327A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201193A>C , CM000668.2:g.157201193A>C	GRCh38
NC_000006.11:g.157522327A>C , CM000668.1:g.157522327A>C	GRCh37
NC_000006.10:g.157564019A>C	NCBI36
NG_032093.1:g.428264A>C
NG_032093.2:g.428264A>C
NG_066624.1:g.430168A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4809A>C	ENSP00000055163.8:p.Thr1603=
ENST00000414678.8:c.4878A>C	ENSP00000412835.3:p.Thr1626=
ENST00000637015.2:c.5097A>C	ENSP00000489729.2:p.Thr1699=
ENST00000346085.10:c.4848A>C	ENSP00000344546.5:p.Thr1616=
ENST00000350026.10:c.4560A>C	ENSP00000055163.7:p.Thr1520=
ENST00000414678.7:c.3126A>C	ENSP00000412835.2:p.Thr1042=
ENST00000635849.1:c.2289A>C	ENSP00000490948.1:p.Thr763=
ENST00000635957.1:c.1920A>C	ENSP00000490385.1:p.Thr640=
ENST00000636227.1:n.3431A>C
ENST00000636254.1:n.888A>C
ENST00000636930.2:c.4968A>C MANE Select	ENSP00000490491.2:p.Thr1656=
ENST00000636940.1:n.2965A>C
ENST00000637015.1:c.2336A>C
ENST00000637568.1:c.2250A>C
ENST00000637741.1:n.1634A>C
ENST00000637810.1:c.2310A>C	ENSP00000489636.1:p.Thr770=
ENST00000637904.1:c.2469A>C	ENSP00000490550.1:p.Thr823=
ENST00000647938.1:c.4599A>C	ENSP00000498155.1:p.Thr1533=
ENST00000346085.9:c.4599A>C	ENSP00000344546.4:p.Thr1533=
ENST00000350026.9:c.4560A>C	ENSP00000055163.7:p.Thr1520=
ENST00000414678.6:c.3126A>C	ENSP00000412835.2:p.Thr1042=
NM_017519.2:c.4560A>C	NP_059989.2:p.Thr1520=
NM_020732.3:c.4599A>C	NP_065783.3:p.Thr1533=
XM_005267069.3:c.4719A>C	XP_005267126.2:p.Thr1573=
XM_011535984.1:c.3798A>C	XP_011534286.1:p.Thr1266=
XM_011535985.1:c.3618A>C	XP_011534287.1:p.Thr1206=
XM_011535986.1:c.3378A>C	XP_011534288.1:p.Thr1126=
XM_011535987.1:c.2997A>C	XP_011534289.1:p.Thr999=
XM_011535988.1:c.1860A>C	XP_011534290.1:p.Thr620=
NM_001346813.1:c.4719A>C	NP_001333742.1:p.Thr1573=
NM_001363725.1:c.2469A>C	NP_001350654.1:p.Thr823=
XM_011535984.2:c.4929A>C	XP_011534286.2:p.Thr1643=
XM_011535988.3:c.1860A>C	XP_011534290.1:p.Thr620=
XM_017011103.2:c.4830A>C	XP_016866592.1:p.Thr1610=
XM_017011104.1:c.4800A>C	XP_016866593.1:p.Thr1600=
XM_017011105.2:c.4770A>C	XP_016866594.1:p.Thr1590=
XM_017011106.2:c.4641A>C	XP_016866595.1:p.Thr1547=
XM_017011107.2:c.4620A>C	XP_016866596.1:p.Thr1540=
XR_002956289.1:n.4915A>C
NM_001363725.2:c.2469A>C	NP_001350654.1:p.Thr823=
NM_001371656.1:c.4848A>C	NP_001358585.1:p.Thr1616=
NM_001374820.1:c.4848A>C	NP_001361749.1:p.Thr1616=
NM_001374828.1:c.4968A>C MANE Select	NP_001361757.1:p.Thr1656=
NM_017519.3:c.4809A>C	NP_059989.3:p.Thr1603=