Canonical Allele Identifier: CA452978424

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522213C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201079C>T , CM000668.2:g.157201079C>T	GRCh38
NC_000006.11:g.157522213C>T , CM000668.1:g.157522213C>T	GRCh37
NC_000006.10:g.157563905C>T	NCBI36
NG_032093.1:g.428150C>T
NG_032093.2:g.428150C>T
NG_066624.1:g.430054C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4695C>T	ENSP00000055163.8:p.Arg1565=
ENST00000414678.8:c.4764C>T	ENSP00000412835.3:p.Arg1588=
ENST00000637015.2:c.4983C>T	ENSP00000489729.2:p.Arg1661=
ENST00000346085.10:c.4734C>T	ENSP00000344546.5:p.Arg1578=
ENST00000350026.10:c.4446C>T	ENSP00000055163.7:p.Arg1482=
ENST00000414678.7:c.3012C>T	ENSP00000412835.2:p.Arg1004=
ENST00000635849.1:c.2175C>T	ENSP00000490948.1:p.Arg725=
ENST00000635957.1:c.1806C>T	ENSP00000490385.1:p.Arg602=
ENST00000636227.1:n.3317C>T
ENST00000636254.1:n.774C>T
ENST00000636930.2:c.4854C>T MANE Select	ENSP00000490491.2:p.Arg1618=
ENST00000636940.1:n.2851C>T
ENST00000637015.1:c.2222C>T
ENST00000637568.1:c.2136C>T
ENST00000637741.1:n.1520C>T
ENST00000637810.1:c.2196C>T	ENSP00000489636.1:p.Arg732=
ENST00000637904.1:c.2355C>T	ENSP00000490550.1:p.Arg785=
ENST00000647938.1:c.4485C>T	ENSP00000498155.1:p.Arg1495=
ENST00000346085.9:c.4485C>T	ENSP00000344546.4:p.Arg1495=
ENST00000350026.9:c.4446C>T	ENSP00000055163.7:p.Arg1482=
ENST00000414678.6:c.3012C>T	ENSP00000412835.2:p.Arg1004=
NM_017519.2:c.4446C>T	NP_059989.2:p.Arg1482=
NM_020732.3:c.4485C>T	NP_065783.3:p.Arg1495=
XM_005267069.3:c.4605C>T	XP_005267126.2:p.Arg1535=
XM_011535984.1:c.3684C>T	XP_011534286.1:p.Arg1228=
XM_011535985.1:c.3504C>T	XP_011534287.1:p.Arg1168=
XM_011535986.1:c.3264C>T	XP_011534288.1:p.Arg1088=
XM_011535987.1:c.2883C>T	XP_011534289.1:p.Arg961=
XM_011535988.1:c.1746C>T	XP_011534290.1:p.Arg582=
NM_001346813.1:c.4605C>T	NP_001333742.1:p.Arg1535=
NM_001363725.1:c.2355C>T	NP_001350654.1:p.Arg785=
XM_011535984.2:c.4815C>T	XP_011534286.2:p.Arg1605=
XM_011535988.3:c.1746C>T	XP_011534290.1:p.Arg582=
XM_017011103.2:c.4716C>T	XP_016866592.1:p.Arg1572=
XM_017011104.1:c.4686C>T	XP_016866593.1:p.Arg1562=
XM_017011105.2:c.4656C>T	XP_016866594.1:p.Arg1552=
XM_017011106.2:c.4527C>T	XP_016866595.1:p.Arg1509=
XM_017011107.2:c.4506C>T	XP_016866596.1:p.Arg1502=
XR_002956289.1:n.4801C>T
NM_001363725.2:c.2355C>T	NP_001350654.1:p.Arg785=
NM_001371656.1:c.4734C>T	NP_001358585.1:p.Arg1578=
NM_001374820.1:c.4734C>T	NP_001361749.1:p.Arg1578=
NM_001374828.1:c.4854C>T MANE Select	NP_001361757.1:p.Arg1618=
NM_017519.3:c.4695C>T	NP_059989.3:p.Arg1565=