Canonical Allele Identifier: CA206652

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157167145G>A , CM000668.2:g.157167145G>A	GRCh38
NC_000006.11:g.157488279G>A , CM000668.1:g.157488279G>A	GRCh37
NC_000006.10:g.157529971G>A	NCBI36
NG_032093.1:g.394216G>A
NG_032093.2:g.394216G>A
NG_066624.1:g.396120G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001374828.1:c.3195G>A MANE Select	NP_001361757.1:p.Pro1065=
ENST00000636930.2:c.3195G>A MANE Select	ENSP00000490491.2:p.Pro1065=
NM_001346813.1:c.2946G>A	NP_001333742.1:p.Pro982=
NM_001363725.1:c.696G>A	NP_001350654.1:p.Pro232=
NM_001363725.2:c.696G>A	NP_001350654.1:p.Pro232=
NM_001371656.1:c.3234G>A	NP_001358585.1:p.Pro1078=
NM_001374820.1:c.3234G>A	NP_001361749.1:p.Pro1078=
NM_017519.2:c.2946G>A	NP_059989.2:p.Pro982=
NM_017519.3:c.3195G>A	NP_059989.3:p.Pro1065=
NM_020732.3:c.2985G>A	NP_065783.3:p.Pro995=
ENST00000319584.10:c.1212G>A	ENSP00000313006.6:p.Pro404=
ENST00000319584.11:c.1209G>A	ENSP00000313006.7:p.Pro403=
ENST00000346085.10:c.3234G>A	ENSP00000344546.5:p.Pro1078=
ENST00000346085.9:c.2985G>A	ENSP00000344546.4:p.Pro995=
ENST00000350026.10:c.2946G>A	ENSP00000055163.7:p.Pro982=
ENST00000350026.11:c.3195G>A	ENSP00000055163.8:p.Pro1065=
ENST00000350026.9:c.2946G>A	ENSP00000055163.7:p.Pro982=
ENST00000400790.3:c.147G>A	ENSP00000383596.3:p.Pro49=
ENST00000414678.6:c.1353G>A	ENSP00000412835.2:p.Pro451=
ENST00000414678.7:c.1353G>A	ENSP00000412835.2:p.Pro451=
ENST00000414678.8:c.3105G>A	ENSP00000412835.3:p.Pro1035=
ENST00000478761.3:c.397G>A
ENST00000635849.1:c.516G>A	ENSP00000490948.1:p.Pro172=
ENST00000635957.1:c.150G>A	ENSP00000490385.1:p.Pro50=
ENST00000636426.1:n.359G>A
ENST00000637015.1:c.563G>A
ENST00000637015.2:c.3324G>A	ENSP00000489729.2:p.Pro1108=
ENST00000637568.1:c.477G>A
ENST00000637722.1:n.1131G>A
ENST00000637810.1:c.696G>A	ENSP00000489636.1:p.Pro232=
ENST00000637904.1:c.696G>A	ENSP00000490550.1:p.Pro232=
ENST00000647938.1:c.2985G>A	ENSP00000498155.1:p.Pro995=
XM_005267069.3:c.2946G>A	XP_005267126.2:p.Pro982=
XM_011535984.1:c.2025G>A	XP_011534286.1:p.Pro675=
XM_011535984.2:c.3156G>A	XP_011534286.2:p.Pro1052=
XM_011535985.1:c.1845G>A	XP_011534287.1:p.Pro615=
XM_011535986.1:c.1605G>A	XP_011534288.1:p.Pro535=
XM_011535987.1:c.1224G>A	XP_011534289.1:p.Pro408=
XM_011535988.1:c.87G>A	XP_011534290.1:p.Pro29=
XM_011535988.3:c.87G>A	XP_011534290.1:p.Pro29=
XM_017011103.2:c.3057G>A	XP_016866592.1:p.Pro1019=
XM_017011104.1:c.3027G>A	XP_016866593.1:p.Pro1009=
XM_017011105.2:c.3156G>A	XP_016866594.1:p.Pro1052=
XM_017011106.2:c.3027G>A	XP_016866595.1:p.Pro1009=
XM_017011107.2:c.2847G>A	XP_016866596.1:p.Pro949=
XR_002956289.1:n.3239G>A