Canonical Allele Identifier: CA452978419

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522204C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201070C>G , CM000668.2:g.157201070C>G	GRCh38
NC_000006.11:g.157522204C>G , CM000668.1:g.157522204C>G	GRCh37
NC_000006.10:g.157563896C>G	NCBI36
NG_032093.1:g.428141C>G
NG_032093.2:g.428141C>G
NG_066624.1:g.430045C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4686C>G	ENSP00000055163.8:p.Gly1562=
ENST00000414678.8:c.4755C>G	ENSP00000412835.3:p.Gly1585=
ENST00000637015.2:c.4974C>G	ENSP00000489729.2:p.Gly1658=
ENST00000346085.10:c.4725C>G	ENSP00000344546.5:p.Gly1575=
ENST00000350026.10:c.4437C>G	ENSP00000055163.7:p.Gly1479=
ENST00000414678.7:c.3003C>G	ENSP00000412835.2:p.Gly1001=
ENST00000635849.1:c.2166C>G	ENSP00000490948.1:p.Gly722=
ENST00000635957.1:c.1797C>G	ENSP00000490385.1:p.Gly599=
ENST00000636227.1:n.3308C>G
ENST00000636254.1:n.765C>G
ENST00000636930.2:c.4845C>G MANE Select	ENSP00000490491.2:p.Gly1615=
ENST00000636940.1:n.2842C>G
ENST00000637015.1:c.2213C>G
ENST00000637568.1:c.2127C>G
ENST00000637741.1:n.1511C>G
ENST00000637810.1:c.2187C>G	ENSP00000489636.1:p.Gly729=
ENST00000637904.1:c.2346C>G	ENSP00000490550.1:p.Gly782=
ENST00000647938.1:c.4476C>G	ENSP00000498155.1:p.Gly1492=
ENST00000346085.9:c.4476C>G	ENSP00000344546.4:p.Gly1492=
ENST00000350026.9:c.4437C>G	ENSP00000055163.7:p.Gly1479=
ENST00000414678.6:c.3003C>G	ENSP00000412835.2:p.Gly1001=
NM_017519.2:c.4437C>G	NP_059989.2:p.Gly1479=
NM_020732.3:c.4476C>G	NP_065783.3:p.Gly1492=
XM_005267069.3:c.4596C>G	XP_005267126.2:p.Gly1532=
XM_011535984.1:c.3675C>G	XP_011534286.1:p.Gly1225=
XM_011535985.1:c.3495C>G	XP_011534287.1:p.Gly1165=
XM_011535986.1:c.3255C>G	XP_011534288.1:p.Gly1085=
XM_011535987.1:c.2874C>G	XP_011534289.1:p.Gly958=
XM_011535988.1:c.1737C>G	XP_011534290.1:p.Gly579=
NM_001346813.1:c.4596C>G	NP_001333742.1:p.Gly1532=
NM_001363725.1:c.2346C>G	NP_001350654.1:p.Gly782=
XM_011535984.2:c.4806C>G	XP_011534286.2:p.Gly1602=
XM_011535988.3:c.1737C>G	XP_011534290.1:p.Gly579=
XM_017011103.2:c.4707C>G	XP_016866592.1:p.Gly1569=
XM_017011104.1:c.4677C>G	XP_016866593.1:p.Gly1559=
XM_017011105.2:c.4647C>G	XP_016866594.1:p.Gly1549=
XM_017011106.2:c.4518C>G	XP_016866595.1:p.Gly1506=
XM_017011107.2:c.4497C>G	XP_016866596.1:p.Gly1499=
XR_002956289.1:n.4792C>G
NM_001363725.2:c.2346C>G	NP_001350654.1:p.Gly782=
NM_001371656.1:c.4725C>G	NP_001358585.1:p.Gly1575=
NM_001374820.1:c.4725C>G	NP_001361749.1:p.Gly1575=
NM_001374828.1:c.4845C>G MANE Select	NP_001361757.1:p.Gly1615=
NM_017519.3:c.4686C>G	NP_059989.3:p.Gly1562=