Canonical Allele Identifier: CA452978051

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522241A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201107A>C , CM000668.2:g.157201107A>C	GRCh38
NC_000006.11:g.157522241A>C , CM000668.1:g.157522241A>C	GRCh37
NC_000006.10:g.157563933A>C	NCBI36
NG_032093.1:g.428178A>C
NG_032093.2:g.428178A>C
NG_066624.1:g.430082A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4723A>C	ENSP00000055163.8:p.Arg1575=
ENST00000414678.8:c.4792A>C	ENSP00000412835.3:p.Arg1598=
ENST00000637015.2:c.5011A>C	ENSP00000489729.2:p.Arg1671=
ENST00000346085.10:c.4762A>C	ENSP00000344546.5:p.Arg1588=
ENST00000350026.10:c.4474A>C	ENSP00000055163.7:p.Arg1492=
ENST00000414678.7:c.3040A>C	ENSP00000412835.2:p.Arg1014=
ENST00000635849.1:c.2203A>C	ENSP00000490948.1:p.Arg735=
ENST00000635957.1:c.1834A>C	ENSP00000490385.1:p.Arg612=
ENST00000636227.1:n.3345A>C
ENST00000636254.1:n.802A>C
ENST00000636930.2:c.4882A>C MANE Select	ENSP00000490491.2:p.Arg1628=
ENST00000636940.1:n.2879A>C
ENST00000637015.1:c.2250A>C
ENST00000637568.1:c.2164A>C
ENST00000637741.1:n.1548A>C
ENST00000637810.1:c.2224A>C	ENSP00000489636.1:p.Arg742=
ENST00000637904.1:c.2383A>C	ENSP00000490550.1:p.Arg795=
ENST00000647938.1:c.4513A>C	ENSP00000498155.1:p.Arg1505=
ENST00000346085.9:c.4513A>C	ENSP00000344546.4:p.Arg1505=
ENST00000350026.9:c.4474A>C	ENSP00000055163.7:p.Arg1492=
ENST00000414678.6:c.3040A>C	ENSP00000412835.2:p.Arg1014=
NM_017519.2:c.4474A>C	NP_059989.2:p.Arg1492=
NM_020732.3:c.4513A>C	NP_065783.3:p.Arg1505=
XM_005267069.3:c.4633A>C	XP_005267126.2:p.Arg1545=
XM_011535984.1:c.3712A>C	XP_011534286.1:p.Arg1238=
XM_011535985.1:c.3532A>C	XP_011534287.1:p.Arg1178=
XM_011535986.1:c.3292A>C	XP_011534288.1:p.Arg1098=
XM_011535987.1:c.2911A>C	XP_011534289.1:p.Arg971=
XM_011535988.1:c.1774A>C	XP_011534290.1:p.Arg592=
NM_001346813.1:c.4633A>C	NP_001333742.1:p.Arg1545=
NM_001363725.1:c.2383A>C	NP_001350654.1:p.Arg795=
XM_011535984.2:c.4843A>C	XP_011534286.2:p.Arg1615=
XM_011535988.3:c.1774A>C	XP_011534290.1:p.Arg592=
XM_017011103.2:c.4744A>C	XP_016866592.1:p.Arg1582=
XM_017011104.1:c.4714A>C	XP_016866593.1:p.Arg1572=
XM_017011105.2:c.4684A>C	XP_016866594.1:p.Arg1562=
XM_017011106.2:c.4555A>C	XP_016866595.1:p.Arg1519=
XM_017011107.2:c.4534A>C	XP_016866596.1:p.Arg1512=
XR_002956289.1:n.4829A>C
NM_001363725.2:c.2383A>C	NP_001350654.1:p.Arg795=
NM_001371656.1:c.4762A>C	NP_001358585.1:p.Arg1588=
NM_001374820.1:c.4762A>C	NP_001361749.1:p.Arg1588=
NM_001374828.1:c.4882A>C MANE Select	NP_001361757.1:p.Arg1628=
NM_017519.3:c.4723A>C	NP_059989.3:p.Arg1575=