Canonical Allele Identifier: CA366234035

Gene: ARID1B

Linked Data

• gnomAD v4: 6-157189662-G-A
• MyVariant Identifiers: chr6:g.157510796G>A (hg19) ; chr6:g.157189662G>A (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3781G>A	ENSP00000055163.8:p.Gly1261Ser
ENST00000414678.8:c.3850G>A	ENSP00000412835.3:p.Gly1284Ser
ENST00000637015.2:c.4069G>A	ENSP00000489729.2:p.Gly1357Ser
ENST00000346085.10:c.3820G>A	ENSP00000344546.5:p.Gly1274Ser
ENST00000350026.10:c.3532G>A	ENSP00000055163.7:p.Gly1178Ser
ENST00000414678.7:c.2098G>A	ENSP00000412835.2:p.Gly700Ser
ENST00000635849.1:c.1261G>A	ENSP00000490948.1:p.Gly421Ser
ENST00000635957.1:c.895G>A	ENSP00000490385.1:p.Gly299Ser
ENST00000636930.2:c.3940G>A MANE Select	ENSP00000490491.2:p.Gly1314Ser
ENST00000636940.1:n.1937G>A
ENST00000637015.1:c.1308G>A
ENST00000637568.1:c.1222G>A
ENST00000637741.1:n.606G>A
ENST00000637810.1:c.1282G>A	ENSP00000489636.1:p.Gly428Ser
ENST00000637904.1:c.1441G>A	ENSP00000490550.1:p.Gly481Ser
ENST00000647938.1:c.3571G>A	ENSP00000498155.1:p.Gly1191Ser
ENST00000346085.9:c.3571G>A	ENSP00000344546.4:p.Gly1191Ser
ENST00000350026.9:c.3532G>A	ENSP00000055163.7:p.Gly1178Ser
ENST00000414678.6:c.2098G>A	ENSP00000412835.2:p.Gly700Ser
NM_017519.2:c.3532G>A	NP_059989.2:p.Gly1178Ser
NM_020732.3:c.3571G>A	NP_065783.3:p.Gly1191Ser
XM_005267069.3:c.3691G>A	XP_005267126.2:p.Gly1231Ser
XM_011535984.1:c.2770G>A	XP_011534286.1:p.Gly924Ser
XM_011535985.1:c.2590G>A	XP_011534287.1:p.Gly864Ser
XM_011535986.1:c.2350G>A	XP_011534288.1:p.Gly784Ser
XM_011535987.1:c.1969G>A	XP_011534289.1:p.Gly657Ser
XM_011535988.1:c.832G>A	XP_011534290.1:p.Gly278Ser
NM_001346813.1:c.3691G>A	NP_001333742.1:p.Gly1231Ser
NM_001363725.1:c.1441G>A	NP_001350654.1:p.Gly481Ser
XM_011535984.2:c.3901G>A	XP_011534286.2:p.Gly1301Ser
XM_011535988.3:c.832G>A	XP_011534290.1:p.Gly278Ser
XM_017011103.2:c.3802G>A	XP_016866592.1:p.Gly1268Ser
XM_017011104.1:c.3772G>A	XP_016866593.1:p.Gly1258Ser
XM_017011105.2:c.3742G>A	XP_016866594.1:p.Gly1248Ser
XM_017011106.2:c.3613G>A	XP_016866595.1:p.Gly1205Ser
XM_017011107.2:c.3592G>A	XP_016866596.1:p.Gly1198Ser
XR_002956289.1:n.3984G>A
NM_001363725.2:c.1441G>A	NP_001350654.1:p.Gly481Ser
NM_001371656.1:c.3820G>A	NP_001358585.1:p.Gly1274Ser
NM_001374820.1:c.3820G>A	NP_001361749.1:p.Gly1274Ser
NM_001374828.1:c.3940G>A MANE Select	NP_001361757.1:p.Gly1314Ser
NM_017519.3:c.3781G>A	NP_059989.3:p.Gly1261Ser