Canonical Allele Identifier: CA1675523376

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201311C= , CM000668.2:g.157201311C=	GRCh38
NC_000006.11:g.157522445C= , CM000668.1:g.157522445C=	GRCh37
NC_000006.10:g.157564137C=	NCBI36
NG_032093.1:g.428382C=
NG_032093.2:g.428382C=
NG_066624.1:g.430286C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4927C=	ENSP00000055163.8:p.Pro1643=
ENST00000414678.8:c.4996C=	ENSP00000412835.3:p.Pro1666=
ENST00000637015.2:c.5215C=	ENSP00000489729.2:p.Pro1739=
ENST00000346085.10:c.4966C=	ENSP00000344546.5:p.Pro1656=
ENST00000350026.10:c.4678C=	ENSP00000055163.7:p.Pro1560=
ENST00000414678.7:c.3244C=	ENSP00000412835.2:p.Pro1082=
ENST00000635849.1:c.2407C=	ENSP00000490948.1:p.Pro803=
ENST00000635957.1:c.2038C=	ENSP00000490385.1:p.Pro680=
ENST00000636227.1:n.3549C=
ENST00000636254.1:n.1006C=
ENST00000636930.2:c.5086C= MANE Select	ENSP00000490491.2:p.Pro1696=
ENST00000636940.1:n.3083C=
ENST00000637015.1:c.2454C=
ENST00000637568.1:c.2368C=
ENST00000637741.1:n.1752C=
ENST00000637810.1:c.2428C=	ENSP00000489636.1:p.Pro810=
ENST00000637904.1:c.2587C=	ENSP00000490550.1:p.Pro863=
ENST00000647938.1:c.4717C=	ENSP00000498155.1:p.Pro1573=
ENST00000346085.9:c.4717C=	ENSP00000344546.4:p.Pro1573=
ENST00000350026.9:c.4678C=	ENSP00000055163.7:p.Pro1560=
ENST00000414678.6:c.3244C=	ENSP00000412835.2:p.Pro1082=
NM_017519.2:c.4678C=	NP_059989.2:p.Pro1560=
NM_020732.3:c.4717C=	NP_065783.3:p.Pro1573=
XM_005267069.3:c.4837C=	XP_005267126.2:p.Pro1613=
XM_011535984.1:c.3916C=	XP_011534286.1:p.Pro1306=
XM_011535985.1:c.3736C=	XP_011534287.1:p.Pro1246=
XM_011535986.1:c.3496C=	XP_011534288.1:p.Pro1166=
XM_011535987.1:c.3115C=	XP_011534289.1:p.Pro1039=
XM_011535988.1:c.1978C=	XP_011534290.1:p.Pro660=
NM_001346813.1:c.4837C=	NP_001333742.1:p.Pro1613=
NM_001363725.1:c.2587C=	NP_001350654.1:p.Pro863=
XM_011535984.2:c.5047C=	XP_011534286.2:p.Pro1683=
XM_011535988.3:c.1978C=	XP_011534290.1:p.Pro660=
XM_017011103.2:c.4948C=	XP_016866592.1:p.Pro1650=
XM_017011104.1:c.4918C=	XP_016866593.1:p.Pro1640=
XM_017011105.2:c.4888C=	XP_016866594.1:p.Pro1630=
XM_017011106.2:c.4759C=	XP_016866595.1:p.Pro1587=
XM_017011107.2:c.4738C=	XP_016866596.1:p.Pro1580=
XR_002956289.1:n.5033C=
NM_001363725.2:c.2587C=	NP_001350654.1:p.Pro863=
NM_001371656.1:c.4966C=	NP_001358585.1:p.Pro1656=
NM_001374820.1:c.4966C=	NP_001361749.1:p.Pro1656=
NM_001374828.1:c.5086C= MANE Select	NP_001361757.1:p.Pro1696=
NM_017519.3:c.4927C=	NP_059989.3:p.Pro1643=