Canonical Allele Identifier: CA366227385

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128316936
• MyVariant Identifiers: chr6:g.157502164A>T (hg19) ; chr6:g.157181030A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181030A>T , CM000668.2:g.157181030A>T	GRCh38
NC_000006.11:g.157502164A>T , CM000668.1:g.157502164A>T	GRCh37
NC_000006.10:g.157543856A>T	NCBI36
NG_032093.1:g.408101A>T
NG_032093.2:g.408101A>T
NG_066624.1:g.410005A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3407A>T	ENSP00000055163.8:p.Glu1136Val
ENST00000414678.8:c.3476A>T	ENSP00000412835.3:p.Glu1159Val
ENST00000637015.2:c.3695A>T	ENSP00000489729.2:p.Glu1232Val
ENST00000319584.11:c.1580A>T	ENSP00000313006.7:p.Glu527Val
ENST00000346085.10:c.3446A>T	ENSP00000344546.5:p.Glu1149Val
ENST00000350026.10:c.3158A>T	ENSP00000055163.7:p.Glu1053Val
ENST00000414678.7:c.1724A>T	ENSP00000412835.2:p.Glu575Val
ENST00000635849.1:c.887A>T	ENSP00000490948.1:p.Glu296Val
ENST00000635957.1:c.521A>T	ENSP00000490385.1:p.Glu174Val
ENST00000636930.2:c.3566A>T MANE Select	ENSP00000490491.2:p.Glu1189Val
ENST00000636940.1:n.1563A>T
ENST00000637015.1:c.934A>T
ENST00000637568.1:c.848A>T
ENST00000637741.1:n.232A>T
ENST00000637810.1:c.908A>T	ENSP00000489636.1:p.Glu303Val
ENST00000637904.1:c.1067A>T	ENSP00000490550.1:p.Glu356Val
ENST00000647938.1:c.3197A>T	ENSP00000498155.1:p.Glu1066Val
ENST00000319584.10:c.1583A>T	ENSP00000313006.6:p.Glu528Val
ENST00000346085.9:c.3197A>T	ENSP00000344546.4:p.Glu1066Val
ENST00000350026.9:c.3158A>T	ENSP00000055163.7:p.Glu1053Val
ENST00000400790.3:c.359A>T	ENSP00000383596.3:p.Glu120Val
ENST00000414678.6:c.1724A>T	ENSP00000412835.2:p.Glu575Val
ENST00000478761.3:c.768A>T
NM_017519.2:c.3158A>T	NP_059989.2:p.Glu1053Val
NM_020732.3:c.3197A>T	NP_065783.3:p.Glu1066Val
XM_005267069.3:c.3317A>T	XP_005267126.2:p.Glu1106Val
XM_011535984.1:c.2396A>T	XP_011534286.1:p.Glu799Val
XM_011535985.1:c.2216A>T	XP_011534287.1:p.Glu739Val
XM_011535986.1:c.1976A>T	XP_011534288.1:p.Glu659Val
XM_011535987.1:c.1595A>T	XP_011534289.1:p.Glu532Val
XM_011535988.1:c.458A>T	XP_011534290.1:p.Glu153Val
NM_001346813.1:c.3317A>T	NP_001333742.1:p.Glu1106Val
NM_001363725.1:c.1067A>T	NP_001350654.1:p.Glu356Val
XM_011535984.2:c.3527A>T	XP_011534286.2:p.Glu1176Val
XM_011535988.3:c.458A>T	XP_011534290.1:p.Glu153Val
XM_017011103.2:c.3428A>T	XP_016866592.1:p.Glu1143Val
XM_017011104.1:c.3398A>T	XP_016866593.1:p.Glu1133Val
XM_017011105.2:c.3368A>T	XP_016866594.1:p.Glu1123Val
XM_017011106.2:c.3239A>T	XP_016866595.1:p.Glu1080Val
XM_017011107.2:c.3218A>T	XP_016866596.1:p.Glu1073Val
XR_002956289.1:n.3610A>T
NM_001363725.2:c.1067A>T	NP_001350654.1:p.Glu356Val
NM_001371656.1:c.3446A>T	NP_001358585.1:p.Glu1149Val
NM_001374820.1:c.3446A>T	NP_001361749.1:p.Glu1149Val
NM_001374828.1:c.3566A>T MANE Select	NP_001361757.1:p.Glu1189Val
NM_017519.3:c.3407A>T	NP_059989.3:p.Glu1136Val