Canonical Allele Identifier: CA452978100

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522276C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201142C>G , CM000668.2:g.157201142C>G	GRCh38
NC_000006.11:g.157522276C>G , CM000668.1:g.157522276C>G	GRCh37
NC_000006.10:g.157563968C>G	NCBI36
NG_032093.1:g.428213C>G
NG_032093.2:g.428213C>G
NG_066624.1:g.430117C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4758C>G	ENSP00000055163.8:p.Val1586=
ENST00000414678.8:c.4827C>G	ENSP00000412835.3:p.Val1609=
ENST00000637015.2:c.5046C>G	ENSP00000489729.2:p.Val1682=
ENST00000346085.10:c.4797C>G	ENSP00000344546.5:p.Val1599=
ENST00000350026.10:c.4509C>G	ENSP00000055163.7:p.Val1503=
ENST00000414678.7:c.3075C>G	ENSP00000412835.2:p.Val1025=
ENST00000635849.1:c.2238C>G	ENSP00000490948.1:p.Val746=
ENST00000635957.1:c.1869C>G	ENSP00000490385.1:p.Val623=
ENST00000636227.1:n.3380C>G
ENST00000636254.1:n.837C>G
ENST00000636930.2:c.4917C>G MANE Select	ENSP00000490491.2:p.Val1639=
ENST00000636940.1:n.2914C>G
ENST00000637015.1:c.2285C>G
ENST00000637568.1:c.2199C>G
ENST00000637741.1:n.1583C>G
ENST00000637810.1:c.2259C>G	ENSP00000489636.1:p.Val753=
ENST00000637904.1:c.2418C>G	ENSP00000490550.1:p.Val806=
ENST00000647938.1:c.4548C>G	ENSP00000498155.1:p.Val1516=
ENST00000346085.9:c.4548C>G	ENSP00000344546.4:p.Val1516=
ENST00000350026.9:c.4509C>G	ENSP00000055163.7:p.Val1503=
ENST00000414678.6:c.3075C>G	ENSP00000412835.2:p.Val1025=
NM_017519.2:c.4509C>G	NP_059989.2:p.Val1503=
NM_020732.3:c.4548C>G	NP_065783.3:p.Val1516=
XM_005267069.3:c.4668C>G	XP_005267126.2:p.Val1556=
XM_011535984.1:c.3747C>G	XP_011534286.1:p.Val1249=
XM_011535985.1:c.3567C>G	XP_011534287.1:p.Val1189=
XM_011535986.1:c.3327C>G	XP_011534288.1:p.Val1109=
XM_011535987.1:c.2946C>G	XP_011534289.1:p.Val982=
XM_011535988.1:c.1809C>G	XP_011534290.1:p.Val603=
NM_001346813.1:c.4668C>G	NP_001333742.1:p.Val1556=
NM_001363725.1:c.2418C>G	NP_001350654.1:p.Val806=
XM_011535984.2:c.4878C>G	XP_011534286.2:p.Val1626=
XM_011535988.3:c.1809C>G	XP_011534290.1:p.Val603=
XM_017011103.2:c.4779C>G	XP_016866592.1:p.Val1593=
XM_017011104.1:c.4749C>G	XP_016866593.1:p.Val1583=
XM_017011105.2:c.4719C>G	XP_016866594.1:p.Val1573=
XM_017011106.2:c.4590C>G	XP_016866595.1:p.Val1530=
XM_017011107.2:c.4569C>G	XP_016866596.1:p.Val1523=
XR_002956289.1:n.4864C>G
NM_001363725.2:c.2418C>G	NP_001350654.1:p.Val806=
NM_001371656.1:c.4797C>G	NP_001358585.1:p.Val1599=
NM_001374820.1:c.4797C>G	NP_001361749.1:p.Val1599=
NM_001374828.1:c.4917C>G MANE Select	NP_001361757.1:p.Val1639=
NM_017519.3:c.4758C>G	NP_059989.3:p.Val1586=