Canonical Allele Identifier: CA366234403

Gene: ARID1B

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3893G>T	ENSP00000055163.8:p.Gly1298Val
ENST00000414678.8:c.3962G>T	ENSP00000412835.3:p.Gly1321Val
ENST00000637015.2:c.4181G>T	ENSP00000489729.2:p.Gly1394Val
ENST00000346085.10:c.3932G>T	ENSP00000344546.5:p.Gly1311Val
ENST00000350026.10:c.3644G>T	ENSP00000055163.7:p.Gly1215Val
ENST00000414678.7:c.2210G>T	ENSP00000412835.2:p.Gly737Val
ENST00000635849.1:c.1373G>T	ENSP00000490948.1:p.Gly458Val
ENST00000635957.1:c.1007G>T	ENSP00000490385.1:p.Gly336Val
ENST00000636930.2:c.4052G>T MANE Select	ENSP00000490491.2:p.Gly1351Val
ENST00000636940.1:n.2049G>T
ENST00000637015.1:c.1420G>T
ENST00000637568.1:c.1334G>T
ENST00000637741.1:n.718G>T
ENST00000637810.1:c.1394G>T	ENSP00000489636.1:p.Gly465Val
ENST00000637904.1:c.1553G>T	ENSP00000490550.1:p.Gly518Val
ENST00000647938.1:c.3683G>T	ENSP00000498155.1:p.Gly1228Val
ENST00000346085.9:c.3683G>T	ENSP00000344546.4:p.Gly1228Val
ENST00000350026.9:c.3644G>T	ENSP00000055163.7:p.Gly1215Val
ENST00000414678.6:c.2210G>T	ENSP00000412835.2:p.Gly737Val
NM_017519.2:c.3644G>T	NP_059989.2:p.Gly1215Val
NM_020732.3:c.3683G>T	NP_065783.3:p.Gly1228Val
XM_005267069.3:c.3803G>T	XP_005267126.2:p.Gly1268Val
XM_011535984.1:c.2882G>T	XP_011534286.1:p.Gly961Val
XM_011535985.1:c.2702G>T	XP_011534287.1:p.Gly901Val
XM_011535986.1:c.2462G>T	XP_011534288.1:p.Gly821Val
XM_011535987.1:c.2081G>T	XP_011534289.1:p.Gly694Val
XM_011535988.1:c.944G>T	XP_011534290.1:p.Gly315Val
NM_001346813.1:c.3803G>T	NP_001333742.1:p.Gly1268Val
NM_001363725.1:c.1553G>T	NP_001350654.1:p.Gly518Val
XM_011535984.2:c.4013G>T	XP_011534286.2:p.Gly1338Val
XM_011535988.3:c.944G>T	XP_011534290.1:p.Gly315Val
XM_017011103.2:c.3914G>T	XP_016866592.1:p.Gly1305Val
XM_017011104.1:c.3884G>T	XP_016866593.1:p.Gly1295Val
XM_017011105.2:c.3854G>T	XP_016866594.1:p.Gly1285Val
XM_017011106.2:c.3725G>T	XP_016866595.1:p.Gly1242Val
XM_017011107.2:c.3704G>T	XP_016866596.1:p.Gly1235Val
XR_002956289.1:n.4096G>T
NM_001363725.2:c.1553G>T	NP_001350654.1:p.Gly518Val
NM_001371656.1:c.3932G>T	NP_001358585.1:p.Gly1311Val
NM_001374820.1:c.3932G>T	NP_001361749.1:p.Gly1311Val
NM_001374828.1:c.4052G>T MANE Select	NP_001361757.1:p.Gly1351Val
NM_017519.3:c.3893G>T	NP_059989.3:p.Gly1298Val