Canonical Allele Identifier: CA366234081

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510818C>G (hg19) ; chr6:g.157189684C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189684C>G , CM000668.2:g.157189684C>G	GRCh38
NC_000006.11:g.157510818C>G , CM000668.1:g.157510818C>G	GRCh37
NC_000006.10:g.157552510C>G	NCBI36
NG_032093.1:g.416755C>G
NG_032093.2:g.416755C>G
NG_066624.1:g.418659C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3803C>G	ENSP00000055163.8:p.Thr1268Ser
ENST00000414678.8:c.3872C>G	ENSP00000412835.3:p.Thr1291Ser
ENST00000637015.2:c.4091C>G	ENSP00000489729.2:p.Thr1364Ser
ENST00000346085.10:c.3842C>G	ENSP00000344546.5:p.Thr1281Ser
ENST00000350026.10:c.3554C>G	ENSP00000055163.7:p.Thr1185Ser
ENST00000414678.7:c.2120C>G	ENSP00000412835.2:p.Thr707Ser
ENST00000635849.1:c.1283C>G	ENSP00000490948.1:p.Thr428Ser
ENST00000635957.1:c.917C>G	ENSP00000490385.1:p.Thr306Ser
ENST00000636930.2:c.3962C>G MANE Select	ENSP00000490491.2:p.Thr1321Ser
ENST00000636940.1:n.1959C>G
ENST00000637015.1:c.1330C>G
ENST00000637568.1:c.1244C>G
ENST00000637741.1:n.628C>G
ENST00000637810.1:c.1304C>G	ENSP00000489636.1:p.Thr435Ser
ENST00000637904.1:c.1463C>G	ENSP00000490550.1:p.Thr488Ser
ENST00000647938.1:c.3593C>G	ENSP00000498155.1:p.Thr1198Ser
ENST00000346085.9:c.3593C>G	ENSP00000344546.4:p.Thr1198Ser
ENST00000350026.9:c.3554C>G	ENSP00000055163.7:p.Thr1185Ser
ENST00000414678.6:c.2120C>G	ENSP00000412835.2:p.Thr707Ser
NM_017519.2:c.3554C>G	NP_059989.2:p.Thr1185Ser
NM_020732.3:c.3593C>G	NP_065783.3:p.Thr1198Ser
XM_005267069.3:c.3713C>G	XP_005267126.2:p.Thr1238Ser
XM_011535984.1:c.2792C>G	XP_011534286.1:p.Thr931Ser
XM_011535985.1:c.2612C>G	XP_011534287.1:p.Thr871Ser
XM_011535986.1:c.2372C>G	XP_011534288.1:p.Thr791Ser
XM_011535987.1:c.1991C>G	XP_011534289.1:p.Thr664Ser
XM_011535988.1:c.854C>G	XP_011534290.1:p.Thr285Ser
NM_001346813.1:c.3713C>G	NP_001333742.1:p.Thr1238Ser
NM_001363725.1:c.1463C>G	NP_001350654.1:p.Thr488Ser
XM_011535984.2:c.3923C>G	XP_011534286.2:p.Thr1308Ser
XM_011535988.3:c.854C>G	XP_011534290.1:p.Thr285Ser
XM_017011103.2:c.3824C>G	XP_016866592.1:p.Thr1275Ser
XM_017011104.1:c.3794C>G	XP_016866593.1:p.Thr1265Ser
XM_017011105.2:c.3764C>G	XP_016866594.1:p.Thr1255Ser
XM_017011106.2:c.3635C>G	XP_016866595.1:p.Thr1212Ser
XM_017011107.2:c.3614C>G	XP_016866596.1:p.Thr1205Ser
XR_002956289.1:n.4006C>G
NM_001363725.2:c.1463C>G	NP_001350654.1:p.Thr488Ser
NM_001371656.1:c.3842C>G	NP_001358585.1:p.Thr1281Ser
NM_001374820.1:c.3842C>G	NP_001361749.1:p.Thr1281Ser
NM_001374828.1:c.3962C>G MANE Select	NP_001361757.1:p.Thr1321Ser
NM_017519.3:c.3803C>G	NP_059989.3:p.Thr1268Ser