Canonical Allele Identifier: CA366242125

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522288G>C (hg19) ; chr6:g.157201154G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201154G>C , CM000668.2:g.157201154G>C	GRCh38
NC_000006.11:g.157522288G>C , CM000668.1:g.157522288G>C	GRCh37
NC_000006.10:g.157563980G>C	NCBI36
NG_032093.1:g.428225G>C
NG_032093.2:g.428225G>C
NG_066624.1:g.430129G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4770G>C	ENSP00000055163.8:p.Gln1590His
ENST00000414678.8:c.4839G>C	ENSP00000412835.3:p.Gln1613His
ENST00000637015.2:c.5058G>C	ENSP00000489729.2:p.Gln1686His
ENST00000346085.10:c.4809G>C	ENSP00000344546.5:p.Gln1603His
ENST00000350026.10:c.4521G>C	ENSP00000055163.7:p.Gln1507His
ENST00000414678.7:c.3087G>C	ENSP00000412835.2:p.Gln1029His
ENST00000635849.1:c.2250G>C	ENSP00000490948.1:p.Gln750His
ENST00000635957.1:c.1881G>C	ENSP00000490385.1:p.Gln627His
ENST00000636227.1:n.3392G>C
ENST00000636254.1:n.849G>C
ENST00000636930.2:c.4929G>C MANE Select	ENSP00000490491.2:p.Gln1643His
ENST00000636940.1:n.2926G>C
ENST00000637015.1:c.2297G>C
ENST00000637568.1:c.2211G>C
ENST00000637741.1:n.1595G>C
ENST00000637810.1:c.2271G>C	ENSP00000489636.1:p.Gln757His
ENST00000637904.1:c.2430G>C	ENSP00000490550.1:p.Gln810His
ENST00000647938.1:c.4560G>C	ENSP00000498155.1:p.Gln1520His
ENST00000346085.9:c.4560G>C	ENSP00000344546.4:p.Gln1520His
ENST00000350026.9:c.4521G>C	ENSP00000055163.7:p.Gln1507His
ENST00000414678.6:c.3087G>C	ENSP00000412835.2:p.Gln1029His
NM_017519.2:c.4521G>C	NP_059989.2:p.Gln1507His
NM_020732.3:c.4560G>C	NP_065783.3:p.Gln1520His
XM_005267069.3:c.4680G>C	XP_005267126.2:p.Gln1560His
XM_011535984.1:c.3759G>C	XP_011534286.1:p.Gln1253His
XM_011535985.1:c.3579G>C	XP_011534287.1:p.Gln1193His
XM_011535986.1:c.3339G>C	XP_011534288.1:p.Gln1113His
XM_011535987.1:c.2958G>C	XP_011534289.1:p.Gln986His
XM_011535988.1:c.1821G>C	XP_011534290.1:p.Gln607His
NM_001346813.1:c.4680G>C	NP_001333742.1:p.Gln1560His
NM_001363725.1:c.2430G>C	NP_001350654.1:p.Gln810His
XM_011535984.2:c.4890G>C	XP_011534286.2:p.Gln1630His
XM_011535988.3:c.1821G>C	XP_011534290.1:p.Gln607His
XM_017011103.2:c.4791G>C	XP_016866592.1:p.Gln1597His
XM_017011104.1:c.4761G>C	XP_016866593.1:p.Gln1587His
XM_017011105.2:c.4731G>C	XP_016866594.1:p.Gln1577His
XM_017011106.2:c.4602G>C	XP_016866595.1:p.Gln1534His
XM_017011107.2:c.4581G>C	XP_016866596.1:p.Gln1527His
XR_002956289.1:n.4876G>C
NM_001363725.2:c.2430G>C	NP_001350654.1:p.Gln810His
NM_001371656.1:c.4809G>C	NP_001358585.1:p.Gln1603His
NM_001374820.1:c.4809G>C	NP_001361749.1:p.Gln1603His
NM_001374828.1:c.4929G>C MANE Select	NP_001361757.1:p.Gln1643His
NM_017519.3:c.4770G>C	NP_059989.3:p.Gln1590His