Canonical Allele Identifier: CA366227380

Gene: ARID1B

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3406G>T	ENSP00000055163.8:p.Glu1136Ter
ENST00000414678.8:c.3475G>T	ENSP00000412835.3:p.Glu1159Ter
ENST00000637015.2:c.3694G>T	ENSP00000489729.2:p.Glu1232Ter
ENST00000319584.11:c.1579G>T	ENSP00000313006.7:p.Glu527Ter
ENST00000346085.10:c.3445G>T	ENSP00000344546.5:p.Glu1149Ter
ENST00000350026.10:c.3157G>T	ENSP00000055163.7:p.Glu1053Ter
ENST00000414678.7:c.1723G>T	ENSP00000412835.2:p.Glu575Ter
ENST00000635849.1:c.886G>T	ENSP00000490948.1:p.Glu296Ter
ENST00000635957.1:c.520G>T	ENSP00000490385.1:p.Glu174Ter
ENST00000636930.2:c.3565G>T MANE Select	ENSP00000490491.2:p.Glu1189Ter
ENST00000636940.1:n.1562G>T
ENST00000637015.1:c.933G>T
ENST00000637568.1:c.847G>T
ENST00000637741.1:n.231G>T
ENST00000637810.1:c.907G>T	ENSP00000489636.1:p.Glu303Ter
ENST00000637904.1:c.1066G>T	ENSP00000490550.1:p.Glu356Ter
ENST00000647938.1:c.3196G>T	ENSP00000498155.1:p.Glu1066Ter
ENST00000319584.10:c.1582G>T	ENSP00000313006.6:p.Glu528Ter
ENST00000346085.9:c.3196G>T	ENSP00000344546.4:p.Glu1066Ter
ENST00000350026.9:c.3157G>T	ENSP00000055163.7:p.Glu1053Ter
ENST00000400790.3:c.358G>T	ENSP00000383596.3:p.Glu120Ter
ENST00000414678.6:c.1723G>T	ENSP00000412835.2:p.Glu575Ter
ENST00000478761.3:c.767G>T
NM_017519.2:c.3157G>T	NP_059989.2:p.Glu1053Ter
NM_020732.3:c.3196G>T	NP_065783.3:p.Glu1066Ter
XM_005267069.3:c.3316G>T	XP_005267126.2:p.Glu1106Ter
XM_011535984.1:c.2395G>T	XP_011534286.1:p.Glu799Ter
XM_011535985.1:c.2215G>T	XP_011534287.1:p.Glu739Ter
XM_011535986.1:c.1975G>T	XP_011534288.1:p.Glu659Ter
XM_011535987.1:c.1594G>T	XP_011534289.1:p.Glu532Ter
XM_011535988.1:c.457G>T	XP_011534290.1:p.Glu153Ter
NM_001346813.1:c.3316G>T	NP_001333742.1:p.Glu1106Ter
NM_001363725.1:c.1066G>T	NP_001350654.1:p.Glu356Ter
XM_011535984.2:c.3526G>T	XP_011534286.2:p.Glu1176Ter
XM_011535988.3:c.457G>T	XP_011534290.1:p.Glu153Ter
XM_017011103.2:c.3427G>T	XP_016866592.1:p.Glu1143Ter
XM_017011104.1:c.3397G>T	XP_016866593.1:p.Glu1133Ter
XM_017011105.2:c.3367G>T	XP_016866594.1:p.Glu1123Ter
XM_017011106.2:c.3238G>T	XP_016866595.1:p.Glu1080Ter
XM_017011107.2:c.3217G>T	XP_016866596.1:p.Glu1073Ter
XR_002956289.1:n.3609G>T
NM_001363725.2:c.1066G>T	NP_001350654.1:p.Glu356Ter
NM_001371656.1:c.3445G>T	NP_001358585.1:p.Glu1149Ter
NM_001374820.1:c.3445G>T	NP_001361749.1:p.Glu1149Ter
NM_001374828.1:c.3565G>T MANE Select	NP_001361757.1:p.Glu1189Ter
NM_017519.3:c.3406G>T	NP_059989.3:p.Glu1136Ter