Canonical Allele Identifier: CA452780834

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157502300G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181166G>T , CM000668.2:g.157181166G>T	GRCh38
NC_000006.11:g.157502300G>T , CM000668.1:g.157502300G>T	GRCh37
NC_000006.10:g.157543992G>T	NCBI36
NG_032093.1:g.408237G>T
NG_032093.2:g.408237G>T
NG_066624.1:g.410141G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3543G>T	ENSP00000055163.8:p.Gly1181=
ENST00000414678.8:c.3612G>T	ENSP00000412835.3:p.Gly1204=
ENST00000637015.2:c.3831G>T	ENSP00000489729.2:p.Gly1277=
ENST00000319584.11:c.1716G>T	ENSP00000313006.7:p.Gly572=
ENST00000346085.10:c.3582G>T	ENSP00000344546.5:p.Gly1194=
ENST00000350026.10:c.3294G>T	ENSP00000055163.7:p.Gly1098=
ENST00000414678.7:c.1860G>T	ENSP00000412835.2:p.Gly620=
ENST00000635849.1:c.1023G>T	ENSP00000490948.1:p.Gly341=
ENST00000635957.1:c.657G>T	ENSP00000490385.1:p.Gly219=
ENST00000636930.2:c.3702G>T MANE Select	ENSP00000490491.2:p.Gly1234=
ENST00000636940.1:n.1699G>T
ENST00000637015.1:c.1070G>T
ENST00000637568.1:c.984G>T
ENST00000637741.1:n.368G>T
ENST00000637810.1:c.1044G>T	ENSP00000489636.1:p.Gly348=
ENST00000637904.1:c.1203G>T	ENSP00000490550.1:p.Gly401=
ENST00000647938.1:c.3333G>T	ENSP00000498155.1:p.Gly1111=
ENST00000319584.10:c.1719G>T	ENSP00000313006.6:p.Gly573=
ENST00000346085.9:c.3333G>T	ENSP00000344546.4:p.Gly1111=
ENST00000350026.9:c.3294G>T	ENSP00000055163.7:p.Gly1098=
ENST00000400790.3:c.495G>T	ENSP00000383596.3:p.Gly165=
ENST00000414678.6:c.1860G>T	ENSP00000412835.2:p.Gly620=
ENST00000478761.3:c.904G>T
NM_017519.2:c.3294G>T	NP_059989.2:p.Gly1098=
NM_020732.3:c.3333G>T	NP_065783.3:p.Gly1111=
XM_005267069.3:c.3453G>T	XP_005267126.2:p.Gly1151=
XM_011535984.1:c.2532G>T	XP_011534286.1:p.Gly844=
XM_011535985.1:c.2352G>T	XP_011534287.1:p.Gly784=
XM_011535986.1:c.2112G>T	XP_011534288.1:p.Gly704=
XM_011535987.1:c.1731G>T	XP_011534289.1:p.Gly577=
XM_011535988.1:c.594G>T	XP_011534290.1:p.Gly198=
NM_001346813.1:c.3453G>T	NP_001333742.1:p.Gly1151=
NM_001363725.1:c.1203G>T	NP_001350654.1:p.Gly401=
XM_011535984.2:c.3663G>T	XP_011534286.2:p.Gly1221=
XM_011535988.3:c.594G>T	XP_011534290.1:p.Gly198=
XM_017011103.2:c.3564G>T	XP_016866592.1:p.Gly1188=
XM_017011104.1:c.3534G>T	XP_016866593.1:p.Gly1178=
XM_017011105.2:c.3504G>T	XP_016866594.1:p.Gly1168=
XM_017011106.2:c.3375G>T	XP_016866595.1:p.Gly1125=
XM_017011107.2:c.3354G>T	XP_016866596.1:p.Gly1118=
XR_002956289.1:n.3746G>T
NM_001363725.2:c.1203G>T	NP_001350654.1:p.Gly401=
NM_001371656.1:c.3582G>T	NP_001358585.1:p.Gly1194=
NM_001374820.1:c.3582G>T	NP_001361749.1:p.Gly1194=
NM_001374828.1:c.3702G>T MANE Select	NP_001361757.1:p.Gly1234=
NM_017519.3:c.3543G>T	NP_059989.3:p.Gly1181=