Canonical Allele Identifier: CA1675523058

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201149C= , CM000668.2:g.157201149C=	GRCh38
NC_000006.11:g.157522283C= , CM000668.1:g.157522283C=	GRCh37
NC_000006.10:g.157563975C=	NCBI36
NG_032093.1:g.428220C=
NG_032093.2:g.428220C=
NG_066624.1:g.430124C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4765C=	ENSP00000055163.8:p.Arg1589=
ENST00000414678.8:c.4834C=	ENSP00000412835.3:p.Arg1612=
ENST00000637015.2:c.5053C=	ENSP00000489729.2:p.Arg1685=
ENST00000346085.10:c.4804C=	ENSP00000344546.5:p.Arg1602=
ENST00000350026.10:c.4516C=	ENSP00000055163.7:p.Arg1506=
ENST00000414678.7:c.3082C=	ENSP00000412835.2:p.Arg1028=
ENST00000635849.1:c.2245C=	ENSP00000490948.1:p.Arg749=
ENST00000635957.1:c.1876C=	ENSP00000490385.1:p.Arg626=
ENST00000636227.1:n.3387C=
ENST00000636254.1:n.844C=
ENST00000636930.2:c.4924C= MANE Select	ENSP00000490491.2:p.Arg1642=
ENST00000636940.1:n.2921C=
ENST00000637015.1:c.2292C=
ENST00000637568.1:c.2206C=
ENST00000637741.1:n.1590C=
ENST00000637810.1:c.2266C=	ENSP00000489636.1:p.Arg756=
ENST00000637904.1:c.2425C=	ENSP00000490550.1:p.Arg809=
ENST00000647938.1:c.4555C=	ENSP00000498155.1:p.Arg1519=
ENST00000346085.9:c.4555C=	ENSP00000344546.4:p.Arg1519=
ENST00000350026.9:c.4516C=	ENSP00000055163.7:p.Arg1506=
ENST00000414678.6:c.3082C=	ENSP00000412835.2:p.Arg1028=
NM_017519.2:c.4516C=	NP_059989.2:p.Arg1506=
NM_020732.3:c.4555C=	NP_065783.3:p.Arg1519=
XM_005267069.3:c.4675C=	XP_005267126.2:p.Arg1559=
XM_011535984.1:c.3754C=	XP_011534286.1:p.Arg1252=
XM_011535985.1:c.3574C=	XP_011534287.1:p.Arg1192=
XM_011535986.1:c.3334C=	XP_011534288.1:p.Arg1112=
XM_011535987.1:c.2953C=	XP_011534289.1:p.Arg985=
XM_011535988.1:c.1816C=	XP_011534290.1:p.Arg606=
NM_001346813.1:c.4675C=	NP_001333742.1:p.Arg1559=
NM_001363725.1:c.2425C=	NP_001350654.1:p.Arg809=
XM_011535984.2:c.4885C=	XP_011534286.2:p.Arg1629=
XM_011535988.3:c.1816C=	XP_011534290.1:p.Arg606=
XM_017011103.2:c.4786C=	XP_016866592.1:p.Arg1596=
XM_017011104.1:c.4756C=	XP_016866593.1:p.Arg1586=
XM_017011105.2:c.4726C=	XP_016866594.1:p.Arg1576=
XM_017011106.2:c.4597C=	XP_016866595.1:p.Arg1533=
XM_017011107.2:c.4576C=	XP_016866596.1:p.Arg1526=
XR_002956289.1:n.4871C=
NM_001363725.2:c.2425C=	NP_001350654.1:p.Arg809=
NM_001371656.1:c.4804C=	NP_001358585.1:p.Arg1602=
NM_001374820.1:c.4804C=	NP_001361749.1:p.Arg1602=
NM_001374828.1:c.4924C= MANE Select	NP_001361757.1:p.Arg1642=
NM_017519.3:c.4765C=	NP_059989.3:p.Arg1589=