Canonical Allele Identifier: CA452990153

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157469900A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148766A>G , CM000668.2:g.157148766A>G	GRCh38
NC_000006.11:g.157469900A>G , CM000668.1:g.157469900A>G	GRCh37
NC_000006.10:g.157511592A>G	NCBI36
NG_032093.1:g.375837A>G
NG_032093.2:g.375837A>G
NG_066624.1:g.377741A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2904A>G	ENSP00000055163.8:p.Arg968=
ENST00000414678.8:c.2814A>G	ENSP00000412835.3:p.Arg938=
ENST00000637015.2:c.2904A>G	ENSP00000489729.2:p.Arg968=
ENST00000319584.11:c.918A>G	ENSP00000313006.7:p.Arg306=
ENST00000346085.10:c.2943A>G	ENSP00000344546.5:p.Arg981=
ENST00000350026.10:c.2655A>G	ENSP00000055163.7:p.Arg885=
ENST00000414678.7:c.1062A>G	ENSP00000412835.2:p.Arg354=
ENST00000452544.2:n.805A>G
ENST00000635849.1:c.225A>G	ENSP00000490948.1:p.Arg75=
ENST00000636426.1:n.38A>G
ENST00000636930.2:c.2904A>G MANE Select	ENSP00000490491.2:p.Arg968=
ENST00000637015.1:c.143A>G
ENST00000637810.1:c.405A>G	ENSP00000489636.1:p.Arg135=
ENST00000637904.1:c.405A>G	ENSP00000490550.1:p.Arg135=
ENST00000647938.1:c.2694A>G	ENSP00000498155.1:p.Arg898=
ENST00000674190.1:n.1653A>G
ENST00000319584.10:c.921A>G	ENSP00000313006.6:p.Arg307=
ENST00000346085.9:c.2694A>G	ENSP00000344546.4:p.Arg898=
ENST00000350026.9:c.2655A>G	ENSP00000055163.7:p.Arg885=
ENST00000414678.6:c.1062A>G	ENSP00000412835.2:p.Arg354=
ENST00000452544.1:n.751A>G
NM_017519.2:c.2655A>G	NP_059989.2:p.Arg885=
NM_020732.3:c.2694A>G	NP_065783.3:p.Arg898=
XM_005267069.3:c.2655A>G	XP_005267126.2:p.Arg885=
XM_011535984.1:c.1605A>G	XP_011534286.1:p.Arg535=
XM_011535985.1:c.1425A>G	XP_011534287.1:p.Arg475=
XM_011535986.1:c.1185A>G	XP_011534288.1:p.Arg395=
XM_011535987.1:c.804A>G	XP_011534289.1:p.Arg268=
XM_011535988.1:c.-20+15559A>G	XP_011534290.1:n.-20+15559A>G
NM_001346813.1:c.2655A>G	NP_001333742.1:p.Arg885=
NM_001363725.1:c.405A>G	NP_001350654.1:p.Arg135=
XM_011535984.2:c.2736A>G	XP_011534286.2:p.Arg912=
XM_011535988.3:c.-20+15559A>G	XP_011534290.1:n.-20+15559A>G
XM_017011103.2:c.2736A>G	XP_016866592.1:p.Arg912=
XM_017011104.1:c.2736A>G	XP_016866593.1:p.Arg912=
XM_017011105.2:c.2736A>G	XP_016866594.1:p.Arg912=
XM_017011106.2:c.2736A>G	XP_016866595.1:p.Arg912=
XM_017011107.2:c.2556A>G	XP_016866596.1:p.Arg852=
XR_002956289.1:n.2819A>G
NM_001363725.2:c.405A>G	NP_001350654.1:p.Arg135=
NM_001371656.1:c.2943A>G	NP_001358585.1:p.Arg981=
NM_001374820.1:c.2943A>G	NP_001361749.1:p.Arg981=
NM_001374828.1:c.2904A>G MANE Select	NP_001361757.1:p.Arg968=
NM_017519.3:c.2904A>G	NP_059989.3:p.Arg968=