Canonical Allele Identifier: CA4067622

Gene: ARID1B

Linked Data

• dbSNP Id: rs779177994
• ExAC: 6:157519945 G / A
• gnomAD v2: 6-157519945-G-A
• gnomAD v3: 6-157198811-G-A
• gnomAD v4: 6-157198811-G-A
• MyVariant Identifiers: chr6:g.157519945G>A (hg19) ; chr6:g.157198811G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157198811G>A , CM000668.2:g.157198811G>A	GRCh38
NC_000006.11:g.157519945G>A , CM000668.1:g.157519945G>A	GRCh37
NC_000006.10:g.157561637G>A	NCBI36
NG_032093.1:g.425882G>A
NG_032093.2:g.425882G>A
NG_066624.1:g.427786G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.4224G>A	ENSP00000055163.8:p.Arg1408=
ENST00000414678.8:c.4293G>A	ENSP00000412835.3:p.Arg1431=
ENST00000637015.2:c.4512G>A	ENSP00000489729.2:p.Arg1504=
ENST00000346085.10:c.4263G>A	ENSP00000344546.5:p.Arg1421=
ENST00000350026.10:c.3975G>A	ENSP00000055163.7:p.Arg1325=
ENST00000414678.7:c.2541G>A	ENSP00000412835.2:p.Arg847=
ENST00000635849.1:c.1704G>A	ENSP00000490948.1:p.Arg568=
ENST00000635957.1:c.1335G>A	ENSP00000490385.1:p.Arg445=
ENST00000636227.1:n.2846G>A
ENST00000636254.1:n.303G>A
ENST00000636930.2:c.4383G>A MANE Select	ENSP00000490491.2:p.Arg1461=
ENST00000636940.1:n.2380G>A
ENST00000637015.1:c.1751G>A
ENST00000637568.1:c.1665G>A
ENST00000637741.1:n.1049G>A
ENST00000637810.1:c.1725G>A	ENSP00000489636.1:p.Arg575=
ENST00000637904.1:c.1884G>A	ENSP00000490550.1:p.Arg628=
ENST00000647938.1:c.4014G>A	ENSP00000498155.1:p.Arg1338=
ENST00000346085.9:c.4014G>A	ENSP00000344546.4:p.Arg1338=
ENST00000350026.9:c.3975G>A	ENSP00000055163.7:p.Arg1325=
ENST00000414678.6:c.2541G>A	ENSP00000412835.2:p.Arg847=
NM_017519.2:c.3975G>A	NP_059989.2:p.Arg1325=
NM_020732.3:c.4014G>A	NP_065783.3:p.Arg1338=
XM_005267069.3:c.4134G>A	XP_005267126.2:p.Arg1378=
XM_011535984.1:c.3213G>A	XP_011534286.1:p.Arg1071=
XM_011535985.1:c.3033G>A	XP_011534287.1:p.Arg1011=
XM_011535986.1:c.2793G>A	XP_011534288.1:p.Arg931=
XM_011535987.1:c.2412G>A	XP_011534289.1:p.Arg804=
XM_011535988.1:c.1275G>A	XP_011534290.1:p.Arg425=
NM_001346813.1:c.4134G>A	NP_001333742.1:p.Arg1378=
NM_001363725.1:c.1884G>A	NP_001350654.1:p.Arg628=
XM_011535984.2:c.4344G>A	XP_011534286.2:p.Arg1448=
XM_011535988.3:c.1275G>A	XP_011534290.1:p.Arg425=
XM_017011103.2:c.4245G>A	XP_016866592.1:p.Arg1415=
XM_017011104.1:c.4215G>A	XP_016866593.1:p.Arg1405=
XM_017011105.2:c.4185G>A	XP_016866594.1:p.Arg1395=
XM_017011106.2:c.4056G>A	XP_016866595.1:p.Arg1352=
XM_017011107.2:c.4035G>A	XP_016866596.1:p.Arg1345=
XR_002956289.1:n.4427-1894G>A
NM_001363725.2:c.1884G>A	NP_001350654.1:p.Arg628=
NM_001371656.1:c.4263G>A	NP_001358585.1:p.Arg1421=
NM_001374820.1:c.4263G>A	NP_001361749.1:p.Arg1421=
NM_001374828.1:c.4383G>A MANE Select	NP_001361757.1:p.Arg1461=
NM_017519.3:c.4224G>A	NP_059989.3:p.Arg1408=