Canonical Allele Identifier: CA4067748

Gene: ARID1B

Linked Data

• dbSNP Id: rs746810545
• ExAC: 6:157522384 G / A
• gnomAD v2: 6-157522384-G-A
• gnomAD v4: 6-157201250-G-A
• MyVariant Identifiers: chr6:g.157522384G>A (hg19) ; chr6:g.157201250G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201250G>A , CM000668.2:g.157201250G>A	GRCh38
NC_000006.11:g.157522384G>A , CM000668.1:g.157522384G>A	GRCh37
NC_000006.10:g.157564076G>A	NCBI36
NG_032093.1:g.428321G>A
NG_032093.2:g.428321G>A
NG_066624.1:g.430225G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4866G>A	ENSP00000055163.8:p.Arg1622=
ENST00000414678.8:c.4935G>A	ENSP00000412835.3:p.Arg1645=
ENST00000637015.2:c.5154G>A	ENSP00000489729.2:p.Arg1718=
ENST00000346085.10:c.4905G>A	ENSP00000344546.5:p.Arg1635=
ENST00000350026.10:c.4617G>A	ENSP00000055163.7:p.Arg1539=
ENST00000414678.7:c.3183G>A	ENSP00000412835.2:p.Arg1061=
ENST00000635849.1:c.2346G>A	ENSP00000490948.1:p.Arg782=
ENST00000635957.1:c.1977G>A	ENSP00000490385.1:p.Arg659=
ENST00000636227.1:n.3488G>A
ENST00000636254.1:n.945G>A
ENST00000636930.2:c.5025G>A MANE Select	ENSP00000490491.2:p.Arg1675=
ENST00000636940.1:n.3022G>A
ENST00000637015.1:c.2393G>A
ENST00000637568.1:c.2307G>A
ENST00000637741.1:n.1691G>A
ENST00000637810.1:c.2367G>A	ENSP00000489636.1:p.Arg789=
ENST00000637904.1:c.2526G>A	ENSP00000490550.1:p.Arg842=
ENST00000647938.1:c.4656G>A	ENSP00000498155.1:p.Arg1552=
ENST00000346085.9:c.4656G>A	ENSP00000344546.4:p.Arg1552=
ENST00000350026.9:c.4617G>A	ENSP00000055163.7:p.Arg1539=
ENST00000414678.6:c.3183G>A	ENSP00000412835.2:p.Arg1061=
NM_017519.2:c.4617G>A	NP_059989.2:p.Arg1539=
NM_020732.3:c.4656G>A	NP_065783.3:p.Arg1552=
XM_005267069.3:c.4776G>A	XP_005267126.2:p.Arg1592=
XM_011535984.1:c.3855G>A	XP_011534286.1:p.Arg1285=
XM_011535985.1:c.3675G>A	XP_011534287.1:p.Arg1225=
XM_011535986.1:c.3435G>A	XP_011534288.1:p.Arg1145=
XM_011535987.1:c.3054G>A	XP_011534289.1:p.Arg1018=
XM_011535988.1:c.1917G>A	XP_011534290.1:p.Arg639=
NM_001346813.1:c.4776G>A	NP_001333742.1:p.Arg1592=
NM_001363725.1:c.2526G>A	NP_001350654.1:p.Arg842=
XM_011535984.2:c.4986G>A	XP_011534286.2:p.Arg1662=
XM_011535988.3:c.1917G>A	XP_011534290.1:p.Arg639=
XM_017011103.2:c.4887G>A	XP_016866592.1:p.Arg1629=
XM_017011104.1:c.4857G>A	XP_016866593.1:p.Arg1619=
XM_017011105.2:c.4827G>A	XP_016866594.1:p.Arg1609=
XM_017011106.2:c.4698G>A	XP_016866595.1:p.Arg1566=
XM_017011107.2:c.4677G>A	XP_016866596.1:p.Arg1559=
XR_002956289.1:n.4972G>A
NM_001363725.2:c.2526G>A	NP_001350654.1:p.Arg842=
NM_001371656.1:c.4905G>A	NP_001358585.1:p.Arg1635=
NM_001374820.1:c.4905G>A	NP_001361749.1:p.Arg1635=
NM_001374828.1:c.5025G>A MANE Select	NP_001361757.1:p.Arg1675=
NM_017519.3:c.4866G>A	NP_059989.3:p.Arg1622=