Canonical Allele Identifier: CA366387497

Gene: ARID1B

Linked Data

• ClinVar Variation Id: 2500746
• ClinVar RCV Id: RCV003225658
• MyVariant Identifiers: chr6:g.157406039G>C (hg19) ; chr6:g.157084905G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157084905G>C , CM000668.2:g.157084905G>C	GRCh38
NC_000006.11:g.157406039G>C , CM000668.1:g.157406039G>C	GRCh37
NC_000006.10:g.157447731G>C	NCBI36
NG_032093.1:g.311976G>C
NG_032093.2:g.311976G>C
NG_066624.1:g.313880G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2491G>C	ENSP00000055163.8:p.Gly831Arg
ENST00000414678.8:c.2491G>C	ENSP00000412835.3:p.Gly831Arg
ENST00000637015.2:c.2491G>C	ENSP00000489729.2:p.Gly831Arg
ENST00000319584.11:c.505G>C	ENSP00000313006.7:p.Gly169Arg
ENST00000346085.10:c.2530G>C	ENSP00000344546.5:p.Gly844Arg
ENST00000350026.10:c.2242G>C	ENSP00000055163.7:p.Gly748Arg
ENST00000414678.7:c.739G>C	ENSP00000412835.2:p.Gly247Arg
ENST00000452544.2:n.392G>C
ENST00000493658.2:n.140G>C
ENST00000635849.1:c.-9G>C	ENSP00000490948.1:n.-9G>C
ENST00000636930.2:c.2491G>C MANE Select	ENSP00000490491.2:p.Gly831Arg
ENST00000637003.1:c.-9G>C	ENSP00000489666.1:n.-9G>C
ENST00000637810.1:c.-9G>C	ENSP00000489636.1:n.-9G>C
ENST00000637904.1:c.-9G>C	ENSP00000490550.1:n.-9G>C
ENST00000647938.1:c.2281G>C	ENSP00000498155.1:p.Gly761Arg
ENST00000674190.1:n.1240G>C
ENST00000319584.10:c.508G>C	ENSP00000313006.6:p.Gly170Arg
ENST00000346085.9:c.2281G>C	ENSP00000344546.4:p.Gly761Arg
ENST00000350026.9:c.2242G>C	ENSP00000055163.7:p.Gly748Arg
ENST00000414678.6:c.739G>C	ENSP00000412835.2:p.Gly247Arg
ENST00000452544.1:n.350G>C
ENST00000493658.1:n.140G>C
NM_017519.2:c.2242G>C	NP_059989.2:p.Gly748Arg
NM_020732.3:c.2281G>C	NP_065783.3:p.Gly761Arg
XM_005267069.3:c.2242G>C	XP_005267126.2:p.Gly748Arg
XM_011535984.1:c.1192G>C	XP_011534286.1:p.Gly398Arg
XM_011535985.1:c.1192G>C	XP_011534287.1:p.Gly398Arg
XM_011535986.1:c.772G>C	XP_011534288.1:p.Gly258Arg
XM_011535987.1:c.391G>C	XP_011534289.1:p.Gly131Arg
NM_001346813.1:c.2242G>C	NP_001333742.1:p.Gly748Arg
NM_001363725.1:c.-9G>C	NP_001350654.1:n.-9G>C
XM_011535984.2:c.2323G>C	XP_011534286.2:p.Gly775Arg
XM_017011103.2:c.2323G>C	XP_016866592.1:p.Gly775Arg
XM_017011104.1:c.2323G>C	XP_016866593.1:p.Gly775Arg
XM_017011105.2:c.2323G>C	XP_016866594.1:p.Gly775Arg
XM_017011106.2:c.2323G>C	XP_016866595.1:p.Gly775Arg
XM_017011107.2:c.2323G>C	XP_016866596.1:p.Gly775Arg
XR_002956289.1:n.2406G>C
NM_001363725.2:c.-9G>C	NP_001350654.1:n.-9G>C
NM_001371656.1:c.2530G>C	NP_001358585.1:p.Gly844Arg
NM_001374820.1:c.2530G>C	NP_001361749.1:p.Gly844Arg
NM_001374828.1:c.2491G>C MANE Select	NP_001361757.1:p.Gly831Arg
NM_017519.3:c.2491G>C	NP_059989.3:p.Gly831Arg