Canonical Allele Identifier: CA366234402

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510908G>A (hg19) ; chr6:g.157189774G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189774G>A , CM000668.2:g.157189774G>A	GRCh38
NC_000006.11:g.157510908G>A , CM000668.1:g.157510908G>A	GRCh37
NC_000006.10:g.157552600G>A	NCBI36
NG_032093.1:g.416845G>A
NG_032093.2:g.416845G>A
NG_066624.1:g.418749G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3893G>A	ENSP00000055163.8:p.Gly1298Asp
ENST00000414678.8:c.3962G>A	ENSP00000412835.3:p.Gly1321Asp
ENST00000637015.2:c.4181G>A	ENSP00000489729.2:p.Gly1394Asp
ENST00000346085.10:c.3932G>A	ENSP00000344546.5:p.Gly1311Asp
ENST00000350026.10:c.3644G>A	ENSP00000055163.7:p.Gly1215Asp
ENST00000414678.7:c.2210G>A	ENSP00000412835.2:p.Gly737Asp
ENST00000635849.1:c.1373G>A	ENSP00000490948.1:p.Gly458Asp
ENST00000635957.1:c.1007G>A	ENSP00000490385.1:p.Gly336Asp
ENST00000636930.2:c.4052G>A MANE Select	ENSP00000490491.2:p.Gly1351Asp
ENST00000636940.1:n.2049G>A
ENST00000637015.1:c.1420G>A
ENST00000637568.1:c.1334G>A
ENST00000637741.1:n.718G>A
ENST00000637810.1:c.1394G>A	ENSP00000489636.1:p.Gly465Asp
ENST00000637904.1:c.1553G>A	ENSP00000490550.1:p.Gly518Asp
ENST00000647938.1:c.3683G>A	ENSP00000498155.1:p.Gly1228Asp
ENST00000346085.9:c.3683G>A	ENSP00000344546.4:p.Gly1228Asp
ENST00000350026.9:c.3644G>A	ENSP00000055163.7:p.Gly1215Asp
ENST00000414678.6:c.2210G>A	ENSP00000412835.2:p.Gly737Asp
NM_017519.2:c.3644G>A	NP_059989.2:p.Gly1215Asp
NM_020732.3:c.3683G>A	NP_065783.3:p.Gly1228Asp
XM_005267069.3:c.3803G>A	XP_005267126.2:p.Gly1268Asp
XM_011535984.1:c.2882G>A	XP_011534286.1:p.Gly961Asp
XM_011535985.1:c.2702G>A	XP_011534287.1:p.Gly901Asp
XM_011535986.1:c.2462G>A	XP_011534288.1:p.Gly821Asp
XM_011535987.1:c.2081G>A	XP_011534289.1:p.Gly694Asp
XM_011535988.1:c.944G>A	XP_011534290.1:p.Gly315Asp
NM_001346813.1:c.3803G>A	NP_001333742.1:p.Gly1268Asp
NM_001363725.1:c.1553G>A	NP_001350654.1:p.Gly518Asp
XM_011535984.2:c.4013G>A	XP_011534286.2:p.Gly1338Asp
XM_011535988.3:c.944G>A	XP_011534290.1:p.Gly315Asp
XM_017011103.2:c.3914G>A	XP_016866592.1:p.Gly1305Asp
XM_017011104.1:c.3884G>A	XP_016866593.1:p.Gly1295Asp
XM_017011105.2:c.3854G>A	XP_016866594.1:p.Gly1285Asp
XM_017011106.2:c.3725G>A	XP_016866595.1:p.Gly1242Asp
XM_017011107.2:c.3704G>A	XP_016866596.1:p.Gly1235Asp
XR_002956289.1:n.4096G>A
NM_001363725.2:c.1553G>A	NP_001350654.1:p.Gly518Asp
NM_001371656.1:c.3932G>A	NP_001358585.1:p.Gly1311Asp
NM_001374820.1:c.3932G>A	NP_001361749.1:p.Gly1311Asp
NM_001374828.1:c.4052G>A MANE Select	NP_001361757.1:p.Gly1351Asp
NM_017519.3:c.3893G>A	NP_059989.3:p.Gly1298Asp