Canonical Allele Identifier: CA1675517086

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148944C= , CM000668.2:g.157148944C=	GRCh38
NC_000006.11:g.157470078C= , CM000668.1:g.157470078C=	GRCh37
NC_000006.10:g.157511770C=	NCBI36
NG_032093.1:g.376015C=
NG_032093.2:g.376015C=
NG_066624.1:g.377919C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3082C=	ENSP00000055163.8:p.Gln1028=
ENST00000414678.8:c.2992C=	ENSP00000412835.3:p.Gln998=
ENST00000637015.2:c.3082C=	ENSP00000489729.2:p.Gln1028=
ENST00000319584.11:c.1096C=	ENSP00000313006.7:p.Gln366=
ENST00000346085.10:c.3121C=	ENSP00000344546.5:p.Gln1041=
ENST00000350026.10:c.2833C=	ENSP00000055163.7:p.Gln945=
ENST00000414678.7:c.1240C=	ENSP00000412835.2:p.Gln414=
ENST00000452544.2:n.983C=
ENST00000635849.1:c.403C=	ENSP00000490948.1:p.Gln135=
ENST00000635957.1:c.37C=	ENSP00000490385.1:p.Gln13=
ENST00000636426.1:n.216C=
ENST00000636930.2:c.3082C= MANE Select	ENSP00000490491.2:p.Gln1028=
ENST00000637015.1:c.321C=
ENST00000637568.1:c.125C=
ENST00000637810.1:c.583C=	ENSP00000489636.1:p.Gln195=
ENST00000637904.1:c.583C=	ENSP00000490550.1:p.Gln195=
ENST00000647938.1:c.2872C=	ENSP00000498155.1:p.Gln958=
ENST00000674190.1:n.1831C=
ENST00000319584.10:c.1099C=	ENSP00000313006.6:p.Gln367=
ENST00000346085.9:c.2872C=	ENSP00000344546.4:p.Gln958=
ENST00000350026.9:c.2833C=	ENSP00000055163.7:p.Gln945=
ENST00000400790.3:c.34C=	ENSP00000383596.3:p.Gln12=
ENST00000414678.6:c.1240C=	ENSP00000412835.2:p.Gln414=
ENST00000452544.1:n.929C=
ENST00000478761.3:c.155C=
NM_017519.2:c.2833C=	NP_059989.2:p.Gln945=
NM_020732.3:c.2872C=	NP_065783.3:p.Gln958=
XM_005267069.3:c.2833C=	XP_005267126.2:p.Gln945=
XM_011535984.1:c.1783C=	XP_011534286.1:p.Gln595=
XM_011535985.1:c.1603C=	XP_011534287.1:p.Gln535=
XM_011535986.1:c.1363C=	XP_011534288.1:p.Gln455=
XM_011535987.1:c.982C=	XP_011534289.1:p.Gln328=
XM_011535988.1:c.-20+15737C=	XP_011534290.1:n.-20+15737C=
NM_001346813.1:c.2833C=	NP_001333742.1:p.Gln945=
NM_001363725.1:c.583C=	NP_001350654.1:p.Gln195=
XM_011535984.2:c.2914C=	XP_011534286.2:p.Gln972=
XM_011535988.3:c.-20+15737C=	XP_011534290.1:n.-20+15737C=
XM_017011103.2:c.2914C=	XP_016866592.1:p.Gln972=
XM_017011104.1:c.2914C=	XP_016866593.1:p.Gln972=
XM_017011105.2:c.2914C=	XP_016866594.1:p.Gln972=
XM_017011106.2:c.2914C=	XP_016866595.1:p.Gln972=
XM_017011107.2:c.2734C=	XP_016866596.1:p.Gln912=
XR_002956289.1:n.2997C=
NM_001363725.2:c.583C=	NP_001350654.1:p.Gln195=
NM_001371656.1:c.3121C=	NP_001358585.1:p.Gln1041=
NM_001374820.1:c.3121C=	NP_001361749.1:p.Gln1041=
NM_001374828.1:c.3082C= MANE Select	NP_001361757.1:p.Gln1028=
NM_017519.3:c.3082C=	NP_059989.3:p.Gln1028=