Canonical Allele Identifier: CA452780775

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128317256
• MyVariant Identifiers: chr6:g.157502213G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181079G>A , CM000668.2:g.157181079G>A	GRCh38
NC_000006.11:g.157502213G>A , CM000668.1:g.157502213G>A	GRCh37
NC_000006.10:g.157543905G>A	NCBI36
NG_032093.1:g.408150G>A
NG_032093.2:g.408150G>A
NG_066624.1:g.410054G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3456G>A	ENSP00000055163.8:p.Glu1152=
ENST00000414678.8:c.3525G>A	ENSP00000412835.3:p.Glu1175=
ENST00000637015.2:c.3744G>A	ENSP00000489729.2:p.Glu1248=
ENST00000319584.11:c.1629G>A	ENSP00000313006.7:p.Glu543=
ENST00000346085.10:c.3495G>A	ENSP00000344546.5:p.Glu1165=
ENST00000350026.10:c.3207G>A	ENSP00000055163.7:p.Glu1069=
ENST00000414678.7:c.1773G>A	ENSP00000412835.2:p.Glu591=
ENST00000635849.1:c.936G>A	ENSP00000490948.1:p.Glu312=
ENST00000635957.1:c.570G>A	ENSP00000490385.1:p.Glu190=
ENST00000636930.2:c.3615G>A MANE Select	ENSP00000490491.2:p.Glu1205=
ENST00000636940.1:n.1612G>A
ENST00000637015.1:c.983G>A
ENST00000637568.1:c.897G>A
ENST00000637741.1:n.281G>A
ENST00000637810.1:c.957G>A	ENSP00000489636.1:p.Glu319=
ENST00000637904.1:c.1116G>A	ENSP00000490550.1:p.Glu372=
ENST00000647938.1:c.3246G>A	ENSP00000498155.1:p.Glu1082=
ENST00000319584.10:c.1632G>A	ENSP00000313006.6:p.Glu544=
ENST00000346085.9:c.3246G>A	ENSP00000344546.4:p.Glu1082=
ENST00000350026.9:c.3207G>A	ENSP00000055163.7:p.Glu1069=
ENST00000400790.3:c.408G>A	ENSP00000383596.3:p.Glu136=
ENST00000414678.6:c.1773G>A	ENSP00000412835.2:p.Glu591=
ENST00000478761.3:c.817G>A
NM_017519.2:c.3207G>A	NP_059989.2:p.Glu1069=
NM_020732.3:c.3246G>A	NP_065783.3:p.Glu1082=
XM_005267069.3:c.3366G>A	XP_005267126.2:p.Glu1122=
XM_011535984.1:c.2445G>A	XP_011534286.1:p.Glu815=
XM_011535985.1:c.2265G>A	XP_011534287.1:p.Glu755=
XM_011535986.1:c.2025G>A	XP_011534288.1:p.Glu675=
XM_011535987.1:c.1644G>A	XP_011534289.1:p.Glu548=
XM_011535988.1:c.507G>A	XP_011534290.1:p.Glu169=
NM_001346813.1:c.3366G>A	NP_001333742.1:p.Glu1122=
NM_001363725.1:c.1116G>A	NP_001350654.1:p.Glu372=
XM_011535984.2:c.3576G>A	XP_011534286.2:p.Glu1192=
XM_011535988.3:c.507G>A	XP_011534290.1:p.Glu169=
XM_017011103.2:c.3477G>A	XP_016866592.1:p.Glu1159=
XM_017011104.1:c.3447G>A	XP_016866593.1:p.Glu1149=
XM_017011105.2:c.3417G>A	XP_016866594.1:p.Glu1139=
XM_017011106.2:c.3288G>A	XP_016866595.1:p.Glu1096=
XM_017011107.2:c.3267G>A	XP_016866596.1:p.Glu1089=
XR_002956289.1:n.3659G>A
NM_001363725.2:c.1116G>A	NP_001350654.1:p.Glu372=
NM_001371656.1:c.3495G>A	NP_001358585.1:p.Glu1165=
NM_001374820.1:c.3495G>A	NP_001361749.1:p.Glu1165=
NM_001374828.1:c.3615G>A MANE Select	NP_001361757.1:p.Glu1205=
NM_017519.3:c.3456G>A	NP_059989.3:p.Glu1152=