Canonical Allele Identifier: CA1675530424

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157206479C= , CM000668.2:g.157206479C=	GRCh38
NC_000006.11:g.157527613C= , CM000668.1:g.157527613C=	GRCh37
NC_000006.10:g.157569305C=	NCBI36
NG_032093.1:g.433550C=
NG_032093.2:g.433550C=
NG_066624.1:g.435454C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001374828.1:c.5707C= MANE Select	NP_001361757.1:p.Gln1903=
ENST00000636930.2:c.5707C= MANE Select	ENSP00000490491.2:p.Gln1903=
NM_001346813.1:c.5458C=	NP_001333742.1:p.Gln1820=
NM_001363725.1:c.3208C=	NP_001350654.1:p.Gln1070=
NM_001363725.2:c.3208C=	NP_001350654.1:p.Gln1070=
NM_001371656.1:c.5587C=	NP_001358585.1:p.Gln1863=
NM_001374820.1:c.5587C=	NP_001361749.1:p.Gln1863=
NM_017519.2:c.5299C=	NP_059989.2:p.Gln1767=
NM_017519.3:c.5548C=	NP_059989.3:p.Gln1850=
NM_020732.3:c.5338C=	NP_065783.3:p.Gln1780=
ENST00000346085.10:c.5587C=	ENSP00000344546.5:p.Gln1863=
ENST00000346085.9:c.5338C=	ENSP00000344546.4:p.Gln1780=
ENST00000350026.10:c.5299C=	ENSP00000055163.7:p.Gln1767=
ENST00000350026.11:c.5548C=	ENSP00000055163.8:p.Gln1850=
ENST00000350026.9:c.5299C=	ENSP00000055163.7:p.Gln1767=
ENST00000414678.6:c.3865C=	ENSP00000412835.2:p.Gln1289=
ENST00000414678.7:c.3865C=	ENSP00000412835.2:p.Gln1289=
ENST00000414678.8:c.5617C=	ENSP00000412835.3:p.Gln1873=
ENST00000635849.1:c.3028C=	ENSP00000490948.1:p.Gln1010=
ENST00000635957.1:c.2659C=	ENSP00000490385.1:p.Gln887=
ENST00000636227.1:n.4170C=
ENST00000636254.1:n.1627C=
ENST00000636940.1:n.3704C=
ENST00000637015.1:c.3075C=
ENST00000637015.2:c.5836C=	ENSP00000489729.2:p.Gln1946=
ENST00000637568.1:c.2989C=
ENST00000637741.1:n.2373C=
ENST00000637810.1:c.3049C=	ENSP00000489636.1:p.Gln1017=
ENST00000637904.1:c.3208C=	ENSP00000490550.1:p.Gln1070=
ENST00000637933.1:n.2822C=
ENST00000647938.1:c.5338C=	ENSP00000498155.1:p.Gln1780=
XM_005267069.3:c.5458C=	XP_005267126.2:p.Gln1820=
XM_011535984.1:c.4537C=	XP_011534286.1:p.Gln1513=
XM_011535984.2:c.5668C=	XP_011534286.2:p.Gln1890=
XM_011535985.1:c.4357C=	XP_011534287.1:p.Gln1453=
XM_011535986.1:c.4117C=	XP_011534288.1:p.Gln1373=
XM_011535987.1:c.3736C=	XP_011534289.1:p.Gln1246=
XM_011535988.1:c.2599C=	XP_011534290.1:p.Gln867=
XM_011535988.3:c.2599C=	XP_011534290.1:p.Gln867=
XM_017011103.2:c.5569C=	XP_016866592.1:p.Gln1857=
XM_017011104.1:c.5539C=	XP_016866593.1:p.Gln1847=
XM_017011105.2:c.5509C=	XP_016866594.1:p.Gln1837=
XM_017011106.2:c.5380C=	XP_016866595.1:p.Gln1794=
XM_017011107.2:c.5359C=	XP_016866596.1:p.Gln1787=
XR_002956289.1:n.5654C=