Canonical Allele Identifier: CA366227383

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157502164A>C (hg19) ; chr6:g.157181030A>C (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3407A>C	ENSP00000055163.8:p.Glu1136Ala
ENST00000414678.8:c.3476A>C	ENSP00000412835.3:p.Glu1159Ala
ENST00000637015.2:c.3695A>C	ENSP00000489729.2:p.Glu1232Ala
ENST00000319584.11:c.1580A>C	ENSP00000313006.7:p.Glu527Ala
ENST00000346085.10:c.3446A>C	ENSP00000344546.5:p.Glu1149Ala
ENST00000350026.10:c.3158A>C	ENSP00000055163.7:p.Glu1053Ala
ENST00000414678.7:c.1724A>C	ENSP00000412835.2:p.Glu575Ala
ENST00000635849.1:c.887A>C	ENSP00000490948.1:p.Glu296Ala
ENST00000635957.1:c.521A>C	ENSP00000490385.1:p.Glu174Ala
ENST00000636930.2:c.3566A>C MANE Select	ENSP00000490491.2:p.Glu1189Ala
ENST00000636940.1:n.1563A>C
ENST00000637015.1:c.934A>C
ENST00000637568.1:c.848A>C
ENST00000637741.1:n.232A>C
ENST00000637810.1:c.908A>C	ENSP00000489636.1:p.Glu303Ala
ENST00000637904.1:c.1067A>C	ENSP00000490550.1:p.Glu356Ala
ENST00000647938.1:c.3197A>C	ENSP00000498155.1:p.Glu1066Ala
ENST00000319584.10:c.1583A>C	ENSP00000313006.6:p.Glu528Ala
ENST00000346085.9:c.3197A>C	ENSP00000344546.4:p.Glu1066Ala
ENST00000350026.9:c.3158A>C	ENSP00000055163.7:p.Glu1053Ala
ENST00000400790.3:c.359A>C	ENSP00000383596.3:p.Glu120Ala
ENST00000414678.6:c.1724A>C	ENSP00000412835.2:p.Glu575Ala
ENST00000478761.3:c.768A>C
NM_017519.2:c.3158A>C	NP_059989.2:p.Glu1053Ala
NM_020732.3:c.3197A>C	NP_065783.3:p.Glu1066Ala
XM_005267069.3:c.3317A>C	XP_005267126.2:p.Glu1106Ala
XM_011535984.1:c.2396A>C	XP_011534286.1:p.Glu799Ala
XM_011535985.1:c.2216A>C	XP_011534287.1:p.Glu739Ala
XM_011535986.1:c.1976A>C	XP_011534288.1:p.Glu659Ala
XM_011535987.1:c.1595A>C	XP_011534289.1:p.Glu532Ala
XM_011535988.1:c.458A>C	XP_011534290.1:p.Glu153Ala
NM_001346813.1:c.3317A>C	NP_001333742.1:p.Glu1106Ala
NM_001363725.1:c.1067A>C	NP_001350654.1:p.Glu356Ala
XM_011535984.2:c.3527A>C	XP_011534286.2:p.Glu1176Ala
XM_011535988.3:c.458A>C	XP_011534290.1:p.Glu153Ala
XM_017011103.2:c.3428A>C	XP_016866592.1:p.Glu1143Ala
XM_017011104.1:c.3398A>C	XP_016866593.1:p.Glu1133Ala
XM_017011105.2:c.3368A>C	XP_016866594.1:p.Glu1123Ala
XM_017011106.2:c.3239A>C	XP_016866595.1:p.Glu1080Ala
XM_017011107.2:c.3218A>C	XP_016866596.1:p.Glu1073Ala
XR_002956289.1:n.3610A>C
NM_001363725.2:c.1067A>C	NP_001350654.1:p.Glu356Ala
NM_001371656.1:c.3446A>C	NP_001358585.1:p.Glu1149Ala
NM_001374820.1:c.3446A>C	NP_001361749.1:p.Glu1149Ala
NM_001374828.1:c.3566A>C MANE Select	NP_001361757.1:p.Glu1189Ala
NM_017519.3:c.3407A>C	NP_059989.3:p.Glu1136Ala