Canonical Allele Identifier: CA366227378

Gene: ARID1B

Linked Data

• dbSNP Id: rs1554231195
• MyVariant Identifiers: chr6:g.157502163G>A (hg19) ; chr6:g.157181029G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181029G>A , CM000668.2:g.157181029G>A	GRCh38
NC_000006.11:g.157502163G>A , CM000668.1:g.157502163G>A	GRCh37
NC_000006.10:g.157543855G>A	NCBI36
NG_032093.1:g.408100G>A
NG_032093.2:g.408100G>A
NG_066624.1:g.410004G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3406G>A	ENSP00000055163.8:p.Glu1136Lys
ENST00000414678.8:c.3475G>A	ENSP00000412835.3:p.Glu1159Lys
ENST00000637015.2:c.3694G>A	ENSP00000489729.2:p.Glu1232Lys
ENST00000319584.11:c.1579G>A	ENSP00000313006.7:p.Glu527Lys
ENST00000346085.10:c.3445G>A	ENSP00000344546.5:p.Glu1149Lys
ENST00000350026.10:c.3157G>A	ENSP00000055163.7:p.Glu1053Lys
ENST00000414678.7:c.1723G>A	ENSP00000412835.2:p.Glu575Lys
ENST00000635849.1:c.886G>A	ENSP00000490948.1:p.Glu296Lys
ENST00000635957.1:c.520G>A	ENSP00000490385.1:p.Glu174Lys
ENST00000636930.2:c.3565G>A MANE Select	ENSP00000490491.2:p.Glu1189Lys
ENST00000636940.1:n.1562G>A
ENST00000637015.1:c.933G>A
ENST00000637568.1:c.847G>A
ENST00000637741.1:n.231G>A
ENST00000637810.1:c.907G>A	ENSP00000489636.1:p.Glu303Lys
ENST00000637904.1:c.1066G>A	ENSP00000490550.1:p.Glu356Lys
ENST00000647938.1:c.3196G>A	ENSP00000498155.1:p.Glu1066Lys
ENST00000319584.10:c.1582G>A	ENSP00000313006.6:p.Glu528Lys
ENST00000346085.9:c.3196G>A	ENSP00000344546.4:p.Glu1066Lys
ENST00000350026.9:c.3157G>A	ENSP00000055163.7:p.Glu1053Lys
ENST00000400790.3:c.358G>A	ENSP00000383596.3:p.Glu120Lys
ENST00000414678.6:c.1723G>A	ENSP00000412835.2:p.Glu575Lys
ENST00000478761.3:c.767G>A
NM_017519.2:c.3157G>A	NP_059989.2:p.Glu1053Lys
NM_020732.3:c.3196G>A	NP_065783.3:p.Glu1066Lys
XM_005267069.3:c.3316G>A	XP_005267126.2:p.Glu1106Lys
XM_011535984.1:c.2395G>A	XP_011534286.1:p.Glu799Lys
XM_011535985.1:c.2215G>A	XP_011534287.1:p.Glu739Lys
XM_011535986.1:c.1975G>A	XP_011534288.1:p.Glu659Lys
XM_011535987.1:c.1594G>A	XP_011534289.1:p.Glu532Lys
XM_011535988.1:c.457G>A	XP_011534290.1:p.Glu153Lys
NM_001346813.1:c.3316G>A	NP_001333742.1:p.Glu1106Lys
NM_001363725.1:c.1066G>A	NP_001350654.1:p.Glu356Lys
XM_011535984.2:c.3526G>A	XP_011534286.2:p.Glu1176Lys
XM_011535988.3:c.457G>A	XP_011534290.1:p.Glu153Lys
XM_017011103.2:c.3427G>A	XP_016866592.1:p.Glu1143Lys
XM_017011104.1:c.3397G>A	XP_016866593.1:p.Glu1133Lys
XM_017011105.2:c.3367G>A	XP_016866594.1:p.Glu1123Lys
XM_017011106.2:c.3238G>A	XP_016866595.1:p.Glu1080Lys
XM_017011107.2:c.3217G>A	XP_016866596.1:p.Glu1073Lys
XR_002956289.1:n.3609G>A
NM_001363725.2:c.1066G>A	NP_001350654.1:p.Glu356Lys
NM_001371656.1:c.3445G>A	NP_001358585.1:p.Glu1149Lys
NM_001374820.1:c.3445G>A	NP_001361749.1:p.Glu1149Lys
NM_001374828.1:c.3565G>A MANE Select	NP_001361757.1:p.Glu1189Lys
NM_017519.3:c.3406G>A	NP_059989.3:p.Glu1136Lys