Canonical Allele Identifier: CA366241298

Gene: ARID1B

Linked Data

• dbSNP Id: rs1354792101
• MyVariant Identifiers: chr6:g.157522087G>C (hg19) ; chr6:g.157200953G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200953G>C , CM000668.2:g.157200953G>C	GRCh38
NC_000006.11:g.157522087G>C , CM000668.1:g.157522087G>C	GRCh37
NC_000006.10:g.157563779G>C	NCBI36
NG_032093.1:g.428024G>C
NG_032093.2:g.428024G>C
NG_066624.1:g.429928G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4569G>C	ENSP00000055163.8:p.Gln1523His
ENST00000414678.8:c.4638G>C	ENSP00000412835.3:p.Gln1546His
ENST00000637015.2:c.4857G>C	ENSP00000489729.2:p.Gln1619His
ENST00000346085.10:c.4608G>C	ENSP00000344546.5:p.Gln1536His
ENST00000350026.10:c.4320G>C	ENSP00000055163.7:p.Gln1440His
ENST00000414678.7:c.2886G>C	ENSP00000412835.2:p.Gln962His
ENST00000635849.1:c.2049G>C	ENSP00000490948.1:p.Gln683His
ENST00000635957.1:c.1680G>C	ENSP00000490385.1:p.Gln560His
ENST00000636227.1:n.3191G>C
ENST00000636254.1:n.648G>C
ENST00000636930.2:c.4728G>C MANE Select	ENSP00000490491.2:p.Gln1576His
ENST00000636940.1:n.2725G>C
ENST00000637015.1:c.2096G>C
ENST00000637568.1:c.2010G>C
ENST00000637741.1:n.1394G>C
ENST00000637810.1:c.2070G>C	ENSP00000489636.1:p.Gln690His
ENST00000637904.1:c.2229G>C	ENSP00000490550.1:p.Gln743His
ENST00000647938.1:c.4359G>C	ENSP00000498155.1:p.Gln1453His
ENST00000346085.9:c.4359G>C	ENSP00000344546.4:p.Gln1453His
ENST00000350026.9:c.4320G>C	ENSP00000055163.7:p.Gln1440His
ENST00000414678.6:c.2886G>C	ENSP00000412835.2:p.Gln962His
NM_017519.2:c.4320G>C	NP_059989.2:p.Gln1440His
NM_020732.3:c.4359G>C	NP_065783.3:p.Gln1453His
XM_005267069.3:c.4479G>C	XP_005267126.2:p.Gln1493His
XM_011535984.1:c.3558G>C	XP_011534286.1:p.Gln1186His
XM_011535985.1:c.3378G>C	XP_011534287.1:p.Gln1126His
XM_011535986.1:c.3138G>C	XP_011534288.1:p.Gln1046His
XM_011535987.1:c.2757G>C	XP_011534289.1:p.Gln919His
XM_011535988.1:c.1620G>C	XP_011534290.1:p.Gln540His
NM_001346813.1:c.4479G>C	NP_001333742.1:p.Gln1493His
NM_001363725.1:c.2229G>C	NP_001350654.1:p.Gln743His
XM_011535984.2:c.4689G>C	XP_011534286.2:p.Gln1563His
XM_011535988.3:c.1620G>C	XP_011534290.1:p.Gln540His
XM_017011103.2:c.4590G>C	XP_016866592.1:p.Gln1530His
XM_017011104.1:c.4560G>C	XP_016866593.1:p.Gln1520His
XM_017011105.2:c.4530G>C	XP_016866594.1:p.Gln1510His
XM_017011106.2:c.4401G>C	XP_016866595.1:p.Gln1467His
XM_017011107.2:c.4380G>C	XP_016866596.1:p.Gln1460His
XR_002956289.1:n.4675G>C
NM_001363725.2:c.2229G>C	NP_001350654.1:p.Gln743His
NM_001371656.1:c.4608G>C	NP_001358585.1:p.Gln1536His
NM_001374820.1:c.4608G>C	NP_001361749.1:p.Gln1536His
NM_001374828.1:c.4728G>C MANE Select	NP_001361757.1:p.Gln1576His
NM_017519.3:c.4569G>C	NP_059989.3:p.Gln1523His