Canonical Allele Identifier: CA1675517080

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148931T= , CM000668.2:g.157148931T=	GRCh38
NC_000006.11:g.157470065T= , CM000668.1:g.157470065T=	GRCh37
NC_000006.10:g.157511757T=	NCBI36
NG_032093.1:g.376002T=
NG_032093.2:g.376002T=
NG_066624.1:g.377906T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3069T=	ENSP00000055163.8:p.Ala1023=
ENST00000414678.8:c.2979T=	ENSP00000412835.3:p.Ala993=
ENST00000637015.2:c.3069T=	ENSP00000489729.2:p.Ala1023=
ENST00000319584.11:c.1083T=	ENSP00000313006.7:p.Ala361=
ENST00000346085.10:c.3108T=	ENSP00000344546.5:p.Ala1036=
ENST00000350026.10:c.2820T=	ENSP00000055163.7:p.Ala940=
ENST00000414678.7:c.1227T=	ENSP00000412835.2:p.Ala409=
ENST00000452544.2:n.970T=
ENST00000635849.1:c.390T=	ENSP00000490948.1:p.Ala130=
ENST00000635957.1:c.24T=	ENSP00000490385.1:p.Ala8=
ENST00000636426.1:n.203T=
ENST00000636930.2:c.3069T= MANE Select	ENSP00000490491.2:p.Ala1023=
ENST00000637015.1:c.308T=
ENST00000637568.1:c.112T=
ENST00000637810.1:c.570T=	ENSP00000489636.1:p.Ala190=
ENST00000637904.1:c.570T=	ENSP00000490550.1:p.Ala190=
ENST00000647938.1:c.2859T=	ENSP00000498155.1:p.Ala953=
ENST00000674190.1:n.1818T=
ENST00000319584.10:c.1086T=	ENSP00000313006.6:p.Ala362=
ENST00000346085.9:c.2859T=	ENSP00000344546.4:p.Ala953=
ENST00000350026.9:c.2820T=	ENSP00000055163.7:p.Ala940=
ENST00000400790.3:c.21T=	ENSP00000383596.3:p.Ala7=
ENST00000414678.6:c.1227T=	ENSP00000412835.2:p.Ala409=
ENST00000452544.1:n.916T=
ENST00000478761.3:c.142T=
NM_017519.2:c.2820T=	NP_059989.2:p.Ala940=
NM_020732.3:c.2859T=	NP_065783.3:p.Ala953=
XM_005267069.3:c.2820T=	XP_005267126.2:p.Ala940=
XM_011535984.1:c.1770T=	XP_011534286.1:p.Ala590=
XM_011535985.1:c.1590T=	XP_011534287.1:p.Ala530=
XM_011535986.1:c.1350T=	XP_011534288.1:p.Ala450=
XM_011535987.1:c.969T=	XP_011534289.1:p.Ala323=
XM_011535988.1:c.-20+15724T=	XP_011534290.1:n.-20+15724T=
NM_001346813.1:c.2820T=	NP_001333742.1:p.Ala940=
NM_001363725.1:c.570T=	NP_001350654.1:p.Ala190=
XM_011535984.2:c.2901T=	XP_011534286.2:p.Ala967=
XM_011535988.3:c.-20+15724T=	XP_011534290.1:n.-20+15724T=
XM_017011103.2:c.2901T=	XP_016866592.1:p.Ala967=
XM_017011104.1:c.2901T=	XP_016866593.1:p.Ala967=
XM_017011105.2:c.2901T=	XP_016866594.1:p.Ala967=
XM_017011106.2:c.2901T=	XP_016866595.1:p.Ala967=
XM_017011107.2:c.2721T=	XP_016866596.1:p.Ala907=
XR_002956289.1:n.2984T=
NM_001363725.2:c.570T=	NP_001350654.1:p.Ala190=
NM_001371656.1:c.3108T=	NP_001358585.1:p.Ala1036=
NM_001374820.1:c.3108T=	NP_001361749.1:p.Ala1036=
NM_001374828.1:c.3069T= MANE Select	NP_001361757.1:p.Ala1023=
NM_017519.3:c.3069T=	NP_059989.3:p.Ala1023=