Canonical Allele Identifier: CA366234036

Gene: ARID1B

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3781G>C	ENSP00000055163.8:p.Gly1261Arg
ENST00000414678.8:c.3850G>C	ENSP00000412835.3:p.Gly1284Arg
ENST00000637015.2:c.4069G>C	ENSP00000489729.2:p.Gly1357Arg
ENST00000346085.10:c.3820G>C	ENSP00000344546.5:p.Gly1274Arg
ENST00000350026.10:c.3532G>C	ENSP00000055163.7:p.Gly1178Arg
ENST00000414678.7:c.2098G>C	ENSP00000412835.2:p.Gly700Arg
ENST00000635849.1:c.1261G>C	ENSP00000490948.1:p.Gly421Arg
ENST00000635957.1:c.895G>C	ENSP00000490385.1:p.Gly299Arg
ENST00000636930.2:c.3940G>C MANE Select	ENSP00000490491.2:p.Gly1314Arg
ENST00000636940.1:n.1937G>C
ENST00000637015.1:c.1308G>C
ENST00000637568.1:c.1222G>C
ENST00000637741.1:n.606G>C
ENST00000637810.1:c.1282G>C	ENSP00000489636.1:p.Gly428Arg
ENST00000637904.1:c.1441G>C	ENSP00000490550.1:p.Gly481Arg
ENST00000647938.1:c.3571G>C	ENSP00000498155.1:p.Gly1191Arg
ENST00000346085.9:c.3571G>C	ENSP00000344546.4:p.Gly1191Arg
ENST00000350026.9:c.3532G>C	ENSP00000055163.7:p.Gly1178Arg
ENST00000414678.6:c.2098G>C	ENSP00000412835.2:p.Gly700Arg
NM_017519.2:c.3532G>C	NP_059989.2:p.Gly1178Arg
NM_020732.3:c.3571G>C	NP_065783.3:p.Gly1191Arg
XM_005267069.3:c.3691G>C	XP_005267126.2:p.Gly1231Arg
XM_011535984.1:c.2770G>C	XP_011534286.1:p.Gly924Arg
XM_011535985.1:c.2590G>C	XP_011534287.1:p.Gly864Arg
XM_011535986.1:c.2350G>C	XP_011534288.1:p.Gly784Arg
XM_011535987.1:c.1969G>C	XP_011534289.1:p.Gly657Arg
XM_011535988.1:c.832G>C	XP_011534290.1:p.Gly278Arg
NM_001346813.1:c.3691G>C	NP_001333742.1:p.Gly1231Arg
NM_001363725.1:c.1441G>C	NP_001350654.1:p.Gly481Arg
XM_011535984.2:c.3901G>C	XP_011534286.2:p.Gly1301Arg
XM_011535988.3:c.832G>C	XP_011534290.1:p.Gly278Arg
XM_017011103.2:c.3802G>C	XP_016866592.1:p.Gly1268Arg
XM_017011104.1:c.3772G>C	XP_016866593.1:p.Gly1258Arg
XM_017011105.2:c.3742G>C	XP_016866594.1:p.Gly1248Arg
XM_017011106.2:c.3613G>C	XP_016866595.1:p.Gly1205Arg
XM_017011107.2:c.3592G>C	XP_016866596.1:p.Gly1198Arg
XR_002956289.1:n.3984G>C
NM_001363725.2:c.1441G>C	NP_001350654.1:p.Gly481Arg
NM_001371656.1:c.3820G>C	NP_001358585.1:p.Gly1274Arg
NM_001374820.1:c.3820G>C	NP_001361749.1:p.Gly1274Arg
NM_001374828.1:c.3940G>C MANE Select	NP_001361757.1:p.Gly1314Arg
NM_017519.3:c.3781G>C	NP_059989.3:p.Gly1261Arg