Canonical Allele Identifier: CA366248008

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157207091G>C , CM000668.2:g.157207091G>C	GRCh38
NC_000006.11:g.157528225G>C , CM000668.1:g.157528225G>C	GRCh37
NC_000006.10:g.157569917G>C	NCBI36
NG_032093.1:g.434162G>C
NG_032093.2:g.434162G>C
NG_066624.1:g.436066G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001374828.1:c.6319G>C MANE Select	NP_001361757.1:p.Glu2107Gln
ENST00000636930.2:c.6319G>C MANE Select	ENSP00000490491.2:p.Glu2107Gln
NM_001346813.1:c.6070G>C	NP_001333742.1:p.Glu2024Gln
NM_001363725.1:c.3820G>C	NP_001350654.1:p.Glu1274Gln
NM_001363725.2:c.3820G>C	NP_001350654.1:p.Glu1274Gln
NM_001371656.1:c.6199G>C	NP_001358585.1:p.Glu2067Gln
NM_001374820.1:c.6199G>C	NP_001361749.1:p.Glu2067Gln
NM_017519.2:c.5911G>C	NP_059989.2:p.Glu1971Gln
NM_017519.3:c.6160G>C	NP_059989.3:p.Glu2054Gln
NM_020732.3:c.5950G>C	NP_065783.3:p.Glu1984Gln
ENST00000346085.10:c.6199G>C	ENSP00000344546.5:p.Glu2067Gln
ENST00000346085.9:c.5950G>C	ENSP00000344546.4:p.Glu1984Gln
ENST00000350026.10:c.5911G>C	ENSP00000055163.7:p.Glu1971Gln
ENST00000350026.11:c.6160G>C	ENSP00000055163.8:p.Glu2054Gln
ENST00000350026.9:c.5911G>C	ENSP00000055163.7:p.Glu1971Gln
ENST00000414678.6:c.4477G>C	ENSP00000412835.2:p.Glu1493Gln
ENST00000414678.7:c.4477G>C	ENSP00000412835.2:p.Glu1493Gln
ENST00000414678.8:c.6229G>C	ENSP00000412835.3:p.Glu2077Gln
ENST00000635849.1:c.3640G>C	ENSP00000490948.1:p.Glu1214Gln
ENST00000635928.1:c.475G>C	ENSP00000489717.1:p.Glu159Gln
ENST00000635957.1:c.3271G>C	ENSP00000490385.1:p.Glu1091Gln
ENST00000636227.1:n.4782G>C
ENST00000636254.1:n.2239G>C
ENST00000636940.1:n.4316G>C
ENST00000637015.1:c.3687G>C
ENST00000637015.2:c.6448G>C	ENSP00000489729.2:p.Glu2150Gln
ENST00000637568.1:c.3601G>C
ENST00000637741.1:n.2985G>C
ENST00000637810.1:c.3661G>C	ENSP00000489636.1:p.Glu1221Gln
ENST00000637904.1:c.3820G>C	ENSP00000490550.1:p.Glu1274Gln
ENST00000637933.1:n.3434G>C
ENST00000647938.1:c.5950G>C	ENSP00000498155.1:p.Glu1984Gln
XM_005267069.3:c.6070G>C	XP_005267126.2:p.Glu2024Gln
XM_011535984.1:c.5149G>C	XP_011534286.1:p.Glu1717Gln
XM_011535984.2:c.6280G>C	XP_011534286.2:p.Glu2094Gln
XM_011535985.1:c.4969G>C	XP_011534287.1:p.Glu1657Gln
XM_011535986.1:c.4729G>C	XP_011534288.1:p.Glu1577Gln
XM_011535987.1:c.4348G>C	XP_011534289.1:p.Glu1450Gln
XM_011535988.1:c.3211G>C	XP_011534290.1:p.Glu1071Gln
XM_011535988.3:c.3211G>C	XP_011534290.1:p.Glu1071Gln
XM_017011103.2:c.6181G>C	XP_016866592.1:p.Glu2061Gln
XM_017011104.1:c.6151G>C	XP_016866593.1:p.Glu2051Gln
XM_017011105.2:c.6121G>C	XP_016866594.1:p.Glu2041Gln
XM_017011106.2:c.5992G>C	XP_016866595.1:p.Glu1998Gln
XM_017011107.2:c.5971G>C	XP_016866596.1:p.Glu1991Gln
XR_002956289.1:n.6266G>C