Canonical Allele Identifier: CA366234037

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510796G>T (hg19) ; chr6:g.157189662G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189662G>T , CM000668.2:g.157189662G>T	GRCh38
NC_000006.11:g.157510796G>T , CM000668.1:g.157510796G>T	GRCh37
NC_000006.10:g.157552488G>T	NCBI36
NG_032093.1:g.416733G>T
NG_032093.2:g.416733G>T
NG_066624.1:g.418637G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3781G>T	ENSP00000055163.8:p.Gly1261Cys
ENST00000414678.8:c.3850G>T	ENSP00000412835.3:p.Gly1284Cys
ENST00000637015.2:c.4069G>T	ENSP00000489729.2:p.Gly1357Cys
ENST00000346085.10:c.3820G>T	ENSP00000344546.5:p.Gly1274Cys
ENST00000350026.10:c.3532G>T	ENSP00000055163.7:p.Gly1178Cys
ENST00000414678.7:c.2098G>T	ENSP00000412835.2:p.Gly700Cys
ENST00000635849.1:c.1261G>T	ENSP00000490948.1:p.Gly421Cys
ENST00000635957.1:c.895G>T	ENSP00000490385.1:p.Gly299Cys
ENST00000636930.2:c.3940G>T MANE Select	ENSP00000490491.2:p.Gly1314Cys
ENST00000636940.1:n.1937G>T
ENST00000637015.1:c.1308G>T
ENST00000637568.1:c.1222G>T
ENST00000637741.1:n.606G>T
ENST00000637810.1:c.1282G>T	ENSP00000489636.1:p.Gly428Cys
ENST00000637904.1:c.1441G>T	ENSP00000490550.1:p.Gly481Cys
ENST00000647938.1:c.3571G>T	ENSP00000498155.1:p.Gly1191Cys
ENST00000346085.9:c.3571G>T	ENSP00000344546.4:p.Gly1191Cys
ENST00000350026.9:c.3532G>T	ENSP00000055163.7:p.Gly1178Cys
ENST00000414678.6:c.2098G>T	ENSP00000412835.2:p.Gly700Cys
NM_017519.2:c.3532G>T	NP_059989.2:p.Gly1178Cys
NM_020732.3:c.3571G>T	NP_065783.3:p.Gly1191Cys
XM_005267069.3:c.3691G>T	XP_005267126.2:p.Gly1231Cys
XM_011535984.1:c.2770G>T	XP_011534286.1:p.Gly924Cys
XM_011535985.1:c.2590G>T	XP_011534287.1:p.Gly864Cys
XM_011535986.1:c.2350G>T	XP_011534288.1:p.Gly784Cys
XM_011535987.1:c.1969G>T	XP_011534289.1:p.Gly657Cys
XM_011535988.1:c.832G>T	XP_011534290.1:p.Gly278Cys
NM_001346813.1:c.3691G>T	NP_001333742.1:p.Gly1231Cys
NM_001363725.1:c.1441G>T	NP_001350654.1:p.Gly481Cys
XM_011535984.2:c.3901G>T	XP_011534286.2:p.Gly1301Cys
XM_011535988.3:c.832G>T	XP_011534290.1:p.Gly278Cys
XM_017011103.2:c.3802G>T	XP_016866592.1:p.Gly1268Cys
XM_017011104.1:c.3772G>T	XP_016866593.1:p.Gly1258Cys
XM_017011105.2:c.3742G>T	XP_016866594.1:p.Gly1248Cys
XM_017011106.2:c.3613G>T	XP_016866595.1:p.Gly1205Cys
XM_017011107.2:c.3592G>T	XP_016866596.1:p.Gly1198Cys
XR_002956289.1:n.3984G>T
NM_001363725.2:c.1441G>T	NP_001350654.1:p.Gly481Cys
NM_001371656.1:c.3820G>T	NP_001358585.1:p.Gly1274Cys
NM_001374820.1:c.3820G>T	NP_001361749.1:p.Gly1274Cys
NM_001374828.1:c.3940G>T MANE Select	NP_001361757.1:p.Gly1314Cys
NM_017519.3:c.3781G>T	NP_059989.3:p.Gly1261Cys