Canonical Allele Identifier: CA1675523486

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201365C= , CM000668.2:g.157201365C=	GRCh38
NC_000006.11:g.157522499C= , CM000668.1:g.157522499C=	GRCh37
NC_000006.10:g.157564191C=	NCBI36
NG_032093.1:g.428436C=
NG_032093.2:g.428436C=
NG_066624.1:g.430340C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4981C=	ENSP00000055163.8:p.Gln1661=
ENST00000414678.8:c.5050C=	ENSP00000412835.3:p.Gln1684=
ENST00000637015.2:c.5269C=	ENSP00000489729.2:p.Gln1757=
ENST00000346085.10:c.5020C=	ENSP00000344546.5:p.Gln1674=
ENST00000350026.10:c.4732C=	ENSP00000055163.7:p.Gln1578=
ENST00000414678.7:c.3298C=	ENSP00000412835.2:p.Gln1100=
ENST00000635849.1:c.2461C=	ENSP00000490948.1:p.Gln821=
ENST00000635957.1:c.2092C=	ENSP00000490385.1:p.Gln698=
ENST00000636227.1:n.3603C=
ENST00000636254.1:n.1060C=
ENST00000636930.2:c.5140C= MANE Select	ENSP00000490491.2:p.Gln1714=
ENST00000636940.1:n.3137C=
ENST00000637015.1:c.2508C=
ENST00000637568.1:c.2422C=
ENST00000637741.1:n.1806C=
ENST00000637810.1:c.2482C=	ENSP00000489636.1:p.Gln828=
ENST00000637904.1:c.2641C=	ENSP00000490550.1:p.Gln881=
ENST00000647938.1:c.4771C=	ENSP00000498155.1:p.Gln1591=
ENST00000346085.9:c.4771C=	ENSP00000344546.4:p.Gln1591=
ENST00000350026.9:c.4732C=	ENSP00000055163.7:p.Gln1578=
ENST00000414678.6:c.3298C=	ENSP00000412835.2:p.Gln1100=
NM_017519.2:c.4732C=	NP_059989.2:p.Gln1578=
NM_020732.3:c.4771C=	NP_065783.3:p.Gln1591=
XM_005267069.3:c.4891C=	XP_005267126.2:p.Gln1631=
XM_011535984.1:c.3970C=	XP_011534286.1:p.Gln1324=
XM_011535985.1:c.3790C=	XP_011534287.1:p.Gln1264=
XM_011535986.1:c.3550C=	XP_011534288.1:p.Gln1184=
XM_011535987.1:c.3169C=	XP_011534289.1:p.Gln1057=
XM_011535988.1:c.2032C=	XP_011534290.1:p.Gln678=
NM_001346813.1:c.4891C=	NP_001333742.1:p.Gln1631=
NM_001363725.1:c.2641C=	NP_001350654.1:p.Gln881=
XM_011535984.2:c.5101C=	XP_011534286.2:p.Gln1701=
XM_011535988.3:c.2032C=	XP_011534290.1:p.Gln678=
XM_017011103.2:c.5002C=	XP_016866592.1:p.Gln1668=
XM_017011104.1:c.4972C=	XP_016866593.1:p.Gln1658=
XM_017011105.2:c.4942C=	XP_016866594.1:p.Gln1648=
XM_017011106.2:c.4813C=	XP_016866595.1:p.Gln1605=
XM_017011107.2:c.4792C=	XP_016866596.1:p.Gln1598=
XR_002956289.1:n.5087C=
NM_001363725.2:c.2641C=	NP_001350654.1:p.Gln881=
NM_001371656.1:c.5020C=	NP_001358585.1:p.Gln1674=
NM_001374820.1:c.5020C=	NP_001361749.1:p.Gln1674=
NM_001374828.1:c.5140C= MANE Select	NP_001361757.1:p.Gln1714=
NM_017519.3:c.4981C=	NP_059989.3:p.Gln1661=