Canonical Allele Identifier: CA366242760

Gene: ARID1B

Linked Data

• ClinVar Variation Id: 2802941
• ClinVar RCV Id: RCV003679246
• dbSNP Id: rs1421604716
• gnomAD v3: 6-157201366-A-C
• gnomAD v4: 6-157201366-A-C
• MyVariant Identifiers: chr6:g.157522500A>C (hg19) ; chr6:g.157201366A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201366A>C , CM000668.2:g.157201366A>C	GRCh38
NC_000006.11:g.157522500A>C , CM000668.1:g.157522500A>C	GRCh37
NC_000006.10:g.157564192A>C	NCBI36
NG_032093.1:g.428437A>C
NG_032093.2:g.428437A>C
NG_066624.1:g.430341A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4982A>C	ENSP00000055163.8:p.Gln1661Pro
ENST00000414678.8:c.5051A>C	ENSP00000412835.3:p.Gln1684Pro
ENST00000637015.2:c.5270A>C	ENSP00000489729.2:p.Gln1757Pro
ENST00000346085.10:c.5021A>C	ENSP00000344546.5:p.Gln1674Pro
ENST00000350026.10:c.4733A>C	ENSP00000055163.7:p.Gln1578Pro
ENST00000414678.7:c.3299A>C	ENSP00000412835.2:p.Gln1100Pro
ENST00000635849.1:c.2462A>C	ENSP00000490948.1:p.Gln821Pro
ENST00000635957.1:c.2093A>C	ENSP00000490385.1:p.Gln698Pro
ENST00000636227.1:n.3604A>C
ENST00000636254.1:n.1061A>C
ENST00000636930.2:c.5141A>C MANE Select	ENSP00000490491.2:p.Gln1714Pro
ENST00000636940.1:n.3138A>C
ENST00000637015.1:c.2509A>C
ENST00000637568.1:c.2423A>C
ENST00000637741.1:n.1807A>C
ENST00000637810.1:c.2483A>C	ENSP00000489636.1:p.Gln828Pro
ENST00000637904.1:c.2642A>C	ENSP00000490550.1:p.Gln881Pro
ENST00000647938.1:c.4772A>C	ENSP00000498155.1:p.Gln1591Pro
ENST00000346085.9:c.4772A>C	ENSP00000344546.4:p.Gln1591Pro
ENST00000350026.9:c.4733A>C	ENSP00000055163.7:p.Gln1578Pro
ENST00000414678.6:c.3299A>C	ENSP00000412835.2:p.Gln1100Pro
NM_017519.2:c.4733A>C	NP_059989.2:p.Gln1578Pro
NM_020732.3:c.4772A>C	NP_065783.3:p.Gln1591Pro
XM_005267069.3:c.4892A>C	XP_005267126.2:p.Gln1631Pro
XM_011535984.1:c.3971A>C	XP_011534286.1:p.Gln1324Pro
XM_011535985.1:c.3791A>C	XP_011534287.1:p.Gln1264Pro
XM_011535986.1:c.3551A>C	XP_011534288.1:p.Gln1184Pro
XM_011535987.1:c.3170A>C	XP_011534289.1:p.Gln1057Pro
XM_011535988.1:c.2033A>C	XP_011534290.1:p.Gln678Pro
NM_001346813.1:c.4892A>C	NP_001333742.1:p.Gln1631Pro
NM_001363725.1:c.2642A>C	NP_001350654.1:p.Gln881Pro
XM_011535984.2:c.5102A>C	XP_011534286.2:p.Gln1701Pro
XM_011535988.3:c.2033A>C	XP_011534290.1:p.Gln678Pro
XM_017011103.2:c.5003A>C	XP_016866592.1:p.Gln1668Pro
XM_017011104.1:c.4973A>C	XP_016866593.1:p.Gln1658Pro
XM_017011105.2:c.4943A>C	XP_016866594.1:p.Gln1648Pro
XM_017011106.2:c.4814A>C	XP_016866595.1:p.Gln1605Pro
XM_017011107.2:c.4793A>C	XP_016866596.1:p.Gln1598Pro
XR_002956289.1:n.5088A>C
NM_001363725.2:c.2642A>C	NP_001350654.1:p.Gln881Pro
NM_001371656.1:c.5021A>C	NP_001358585.1:p.Gln1674Pro
NM_001374820.1:c.5021A>C	NP_001361749.1:p.Gln1674Pro
NM_001374828.1:c.5141A>C MANE Select	NP_001361757.1:p.Gln1714Pro
NM_017519.3:c.4982A>C	NP_059989.3:p.Gln1661Pro