Canonical Allele Identifier: CA4067699

Gene: ARID1B

Linked Data

• dbSNP Id: rs766446706
• ExAC: 6:157522105 G / C
• gnomAD v2: 6-157522105-G-C
• gnomAD v4: 6-157200971-G-C
• MyVariant Identifiers: chr6:g.157522105G>C (hg19) ; chr6:g.157200971G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200971G>C , CM000668.2:g.157200971G>C	GRCh38
NC_000006.11:g.157522105G>C , CM000668.1:g.157522105G>C	GRCh37
NC_000006.10:g.157563797G>C	NCBI36
NG_032093.1:g.428042G>C
NG_032093.2:g.428042G>C
NG_066624.1:g.429946G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4587G>C	ENSP00000055163.8:p.Gly1529=
ENST00000414678.8:c.4656G>C	ENSP00000412835.3:p.Gly1552=
ENST00000637015.2:c.4875G>C	ENSP00000489729.2:p.Gly1625=
ENST00000346085.10:c.4626G>C	ENSP00000344546.5:p.Gly1542=
ENST00000350026.10:c.4338G>C	ENSP00000055163.7:p.Gly1446=
ENST00000414678.7:c.2904G>C	ENSP00000412835.2:p.Gly968=
ENST00000635849.1:c.2067G>C	ENSP00000490948.1:p.Gly689=
ENST00000635957.1:c.1698G>C	ENSP00000490385.1:p.Gly566=
ENST00000636227.1:n.3209G>C
ENST00000636254.1:n.666G>C
ENST00000636930.2:c.4746G>C MANE Select	ENSP00000490491.2:p.Gly1582=
ENST00000636940.1:n.2743G>C
ENST00000637015.1:c.2114G>C
ENST00000637568.1:c.2028G>C
ENST00000637741.1:n.1412G>C
ENST00000637810.1:c.2088G>C	ENSP00000489636.1:p.Gly696=
ENST00000637904.1:c.2247G>C	ENSP00000490550.1:p.Gly749=
ENST00000647938.1:c.4377G>C	ENSP00000498155.1:p.Gly1459=
ENST00000346085.9:c.4377G>C	ENSP00000344546.4:p.Gly1459=
ENST00000350026.9:c.4338G>C	ENSP00000055163.7:p.Gly1446=
ENST00000414678.6:c.2904G>C	ENSP00000412835.2:p.Gly968=
NM_017519.2:c.4338G>C	NP_059989.2:p.Gly1446=
NM_020732.3:c.4377G>C	NP_065783.3:p.Gly1459=
XM_005267069.3:c.4497G>C	XP_005267126.2:p.Gly1499=
XM_011535984.1:c.3576G>C	XP_011534286.1:p.Gly1192=
XM_011535985.1:c.3396G>C	XP_011534287.1:p.Gly1132=
XM_011535986.1:c.3156G>C	XP_011534288.1:p.Gly1052=
XM_011535987.1:c.2775G>C	XP_011534289.1:p.Gly925=
XM_011535988.1:c.1638G>C	XP_011534290.1:p.Gly546=
NM_001346813.1:c.4497G>C	NP_001333742.1:p.Gly1499=
NM_001363725.1:c.2247G>C	NP_001350654.1:p.Gly749=
XM_011535984.2:c.4707G>C	XP_011534286.2:p.Gly1569=
XM_011535988.3:c.1638G>C	XP_011534290.1:p.Gly546=
XM_017011103.2:c.4608G>C	XP_016866592.1:p.Gly1536=
XM_017011104.1:c.4578G>C	XP_016866593.1:p.Gly1526=
XM_017011105.2:c.4548G>C	XP_016866594.1:p.Gly1516=
XM_017011106.2:c.4419G>C	XP_016866595.1:p.Gly1473=
XM_017011107.2:c.4398G>C	XP_016866596.1:p.Gly1466=
XR_002956289.1:n.4693G>C
NM_001363725.2:c.2247G>C	NP_001350654.1:p.Gly749=
NM_001371656.1:c.4626G>C	NP_001358585.1:p.Gly1542=
NM_001374820.1:c.4626G>C	NP_001361749.1:p.Gly1542=
NM_001374828.1:c.4746G>C MANE Select	NP_001361757.1:p.Gly1582=
NM_017519.3:c.4587G>C	NP_059989.3:p.Gly1529=