Canonical Allele Identifier: CA1675517041

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148845C= , CM000668.2:g.157148845C=	GRCh38
NC_000006.11:g.157469979C= , CM000668.1:g.157469979C=	GRCh37
NC_000006.10:g.157511671C=	NCBI36
NG_032093.1:g.375916C=
NG_032093.2:g.375916C=
NG_066624.1:g.377820C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2983C=	ENSP00000055163.8:p.Gln995=
ENST00000414678.8:c.2893C=	ENSP00000412835.3:p.Gln965=
ENST00000637015.2:c.2983C=	ENSP00000489729.2:p.Gln995=
ENST00000319584.11:c.997C=	ENSP00000313006.7:p.Gln333=
ENST00000346085.10:c.3022C=	ENSP00000344546.5:p.Gln1008=
ENST00000350026.10:c.2734C=	ENSP00000055163.7:p.Gln912=
ENST00000414678.7:c.1141C=	ENSP00000412835.2:p.Gln381=
ENST00000452544.2:n.884C=
ENST00000635849.1:c.304C=	ENSP00000490948.1:p.Gln102=
ENST00000636426.1:n.117C=
ENST00000636930.2:c.2983C= MANE Select	ENSP00000490491.2:p.Gln995=
ENST00000637015.1:c.222C=
ENST00000637568.1:c.26C=
ENST00000637810.1:c.484C=	ENSP00000489636.1:p.Gln162=
ENST00000637904.1:c.484C=	ENSP00000490550.1:p.Gln162=
ENST00000647938.1:c.2773C=	ENSP00000498155.1:p.Gln925=
ENST00000674190.1:n.1732C=
ENST00000319584.10:c.1000C=	ENSP00000313006.6:p.Gln334=
ENST00000346085.9:c.2773C=	ENSP00000344546.4:p.Gln925=
ENST00000350026.9:c.2734C=	ENSP00000055163.7:p.Gln912=
ENST00000414678.6:c.1141C=	ENSP00000412835.2:p.Gln381=
ENST00000452544.1:n.830C=
ENST00000478761.3:c.56C=
NM_017519.2:c.2734C=	NP_059989.2:p.Gln912=
NM_020732.3:c.2773C=	NP_065783.3:p.Gln925=
XM_005267069.3:c.2734C=	XP_005267126.2:p.Gln912=
XM_011535984.1:c.1684C=	XP_011534286.1:p.Gln562=
XM_011535985.1:c.1504C=	XP_011534287.1:p.Gln502=
XM_011535986.1:c.1264C=	XP_011534288.1:p.Gln422=
XM_011535987.1:c.883C=	XP_011534289.1:p.Gln295=
XM_011535988.1:c.-20+15638C=	XP_011534290.1:n.-20+15638C=
NM_001346813.1:c.2734C=	NP_001333742.1:p.Gln912=
NM_001363725.1:c.484C=	NP_001350654.1:p.Gln162=
XM_011535984.2:c.2815C=	XP_011534286.2:p.Gln939=
XM_011535988.3:c.-20+15638C=	XP_011534290.1:n.-20+15638C=
XM_017011103.2:c.2815C=	XP_016866592.1:p.Gln939=
XM_017011104.1:c.2815C=	XP_016866593.1:p.Gln939=
XM_017011105.2:c.2815C=	XP_016866594.1:p.Gln939=
XM_017011106.2:c.2815C=	XP_016866595.1:p.Gln939=
XM_017011107.2:c.2635C=	XP_016866596.1:p.Gln879=
XR_002956289.1:n.2898C=
NM_001363725.2:c.484C=	NP_001350654.1:p.Gln162=
NM_001371656.1:c.3022C=	NP_001358585.1:p.Gln1008=
NM_001374820.1:c.3022C=	NP_001361749.1:p.Gln1008=
NM_001374828.1:c.2983C= MANE Select	NP_001361757.1:p.Gln995=
NM_017519.3:c.2983C=	NP_059989.3:p.Gln995=