Canonical Allele Identifier: CA452780762

Gene: ARID1B

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181056C>A , CM000668.2:g.157181056C>A	GRCh38
NC_000006.11:g.157502190C>A , CM000668.1:g.157502190C>A	GRCh37
NC_000006.10:g.157543882C>A	NCBI36
NG_032093.1:g.408127C>A
NG_032093.2:g.408127C>A
NG_066624.1:g.410031C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3433C>A	ENSP00000055163.8:p.Arg1145=
ENST00000414678.8:c.3502C>A	ENSP00000412835.3:p.Arg1168=
ENST00000637015.2:c.3721C>A	ENSP00000489729.2:p.Arg1241=
ENST00000319584.11:c.1606C>A	ENSP00000313006.7:p.Arg536=
ENST00000346085.10:c.3472C>A	ENSP00000344546.5:p.Arg1158=
ENST00000350026.10:c.3184C>A	ENSP00000055163.7:p.Arg1062=
ENST00000414678.7:c.1750C>A	ENSP00000412835.2:p.Arg584=
ENST00000635849.1:c.913C>A	ENSP00000490948.1:p.Arg305=
ENST00000635957.1:c.547C>A	ENSP00000490385.1:p.Arg183=
ENST00000636930.2:c.3592C>A MANE Select	ENSP00000490491.2:p.Arg1198=
ENST00000636940.1:n.1589C>A
ENST00000637015.1:c.960C>A
ENST00000637568.1:c.874C>A
ENST00000637741.1:n.258C>A
ENST00000637810.1:c.934C>A	ENSP00000489636.1:p.Arg312=
ENST00000637904.1:c.1093C>A	ENSP00000490550.1:p.Arg365=
ENST00000647938.1:c.3223C>A	ENSP00000498155.1:p.Arg1075=
ENST00000319584.10:c.1609C>A	ENSP00000313006.6:p.Arg537=
ENST00000346085.9:c.3223C>A	ENSP00000344546.4:p.Arg1075=
ENST00000350026.9:c.3184C>A	ENSP00000055163.7:p.Arg1062=
ENST00000400790.3:c.385C>A	ENSP00000383596.3:p.Arg129=
ENST00000414678.6:c.1750C>A	ENSP00000412835.2:p.Arg584=
ENST00000478761.3:c.794C>A
NM_017519.2:c.3184C>A	NP_059989.2:p.Arg1062=
NM_020732.3:c.3223C>A	NP_065783.3:p.Arg1075=
XM_005267069.3:c.3343C>A	XP_005267126.2:p.Arg1115=
XM_011535984.1:c.2422C>A	XP_011534286.1:p.Arg808=
XM_011535985.1:c.2242C>A	XP_011534287.1:p.Arg748=
XM_011535986.1:c.2002C>A	XP_011534288.1:p.Arg668=
XM_011535987.1:c.1621C>A	XP_011534289.1:p.Arg541=
XM_011535988.1:c.484C>A	XP_011534290.1:p.Arg162=
NM_001346813.1:c.3343C>A	NP_001333742.1:p.Arg1115=
NM_001363725.1:c.1093C>A	NP_001350654.1:p.Arg365=
XM_011535984.2:c.3553C>A	XP_011534286.2:p.Arg1185=
XM_011535988.3:c.484C>A	XP_011534290.1:p.Arg162=
XM_017011103.2:c.3454C>A	XP_016866592.1:p.Arg1152=
XM_017011104.1:c.3424C>A	XP_016866593.1:p.Arg1142=
XM_017011105.2:c.3394C>A	XP_016866594.1:p.Arg1132=
XM_017011106.2:c.3265C>A	XP_016866595.1:p.Arg1089=
XM_017011107.2:c.3244C>A	XP_016866596.1:p.Arg1082=
XR_002956289.1:n.3636C>A
NM_001363725.2:c.1093C>A	NP_001350654.1:p.Arg365=
NM_001371656.1:c.3472C>A	NP_001358585.1:p.Arg1158=
NM_001374820.1:c.3472C>A	NP_001361749.1:p.Arg1158=
NM_001374828.1:c.3592C>A MANE Select	NP_001361757.1:p.Arg1198=
NM_017519.3:c.3433C>A	NP_059989.3:p.Arg1145=