Canonical Allele Identifier: CA1675517066

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148895G= , CM000668.2:g.157148895G=	GRCh38
NC_000006.11:g.157470029G= , CM000668.1:g.157470029G=	GRCh37
NC_000006.10:g.157511721G=	NCBI36
NG_032093.1:g.375966G=
NG_032093.2:g.375966G=
NG_066624.1:g.377870G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3033G=	ENSP00000055163.8:p.Lys1011=
ENST00000414678.8:c.2943G=	ENSP00000412835.3:p.Lys981=
ENST00000637015.2:c.3033G=	ENSP00000489729.2:p.Lys1011=
ENST00000319584.11:c.1047G=	ENSP00000313006.7:p.Lys349=
ENST00000346085.10:c.3072G=	ENSP00000344546.5:p.Lys1024=
ENST00000350026.10:c.2784G=	ENSP00000055163.7:p.Lys928=
ENST00000414678.7:c.1191G=	ENSP00000412835.2:p.Lys397=
ENST00000452544.2:n.934G=
ENST00000635849.1:c.354G=	ENSP00000490948.1:p.Lys118=
ENST00000636426.1:n.167G=
ENST00000636930.2:c.3033G= MANE Select	ENSP00000490491.2:p.Lys1011=
ENST00000637015.1:c.272G=
ENST00000637568.1:c.76G=
ENST00000637810.1:c.534G=	ENSP00000489636.1:p.Lys178=
ENST00000637904.1:c.534G=	ENSP00000490550.1:p.Lys178=
ENST00000647938.1:c.2823G=	ENSP00000498155.1:p.Lys941=
ENST00000674190.1:n.1782G=
ENST00000319584.10:c.1050G=	ENSP00000313006.6:p.Lys350=
ENST00000346085.9:c.2823G=	ENSP00000344546.4:p.Lys941=
ENST00000350026.9:c.2784G=	ENSP00000055163.7:p.Lys928=
ENST00000414678.6:c.1191G=	ENSP00000412835.2:p.Lys397=
ENST00000452544.1:n.880G=
ENST00000478761.3:c.106G=
NM_017519.2:c.2784G=	NP_059989.2:p.Lys928=
NM_020732.3:c.2823G=	NP_065783.3:p.Lys941=
XM_005267069.3:c.2784G=	XP_005267126.2:p.Lys928=
XM_011535984.1:c.1734G=	XP_011534286.1:p.Lys578=
XM_011535985.1:c.1554G=	XP_011534287.1:p.Lys518=
XM_011535986.1:c.1314G=	XP_011534288.1:p.Lys438=
XM_011535987.1:c.933G=	XP_011534289.1:p.Lys311=
XM_011535988.1:c.-20+15688G=	XP_011534290.1:n.-20+15688G=
NM_001346813.1:c.2784G=	NP_001333742.1:p.Lys928=
NM_001363725.1:c.534G=	NP_001350654.1:p.Lys178=
XM_011535984.2:c.2865G=	XP_011534286.2:p.Lys955=
XM_011535988.3:c.-20+15688G=	XP_011534290.1:n.-20+15688G=
XM_017011103.2:c.2865G=	XP_016866592.1:p.Lys955=
XM_017011104.1:c.2865G=	XP_016866593.1:p.Lys955=
XM_017011105.2:c.2865G=	XP_016866594.1:p.Lys955=
XM_017011106.2:c.2865G=	XP_016866595.1:p.Lys955=
XM_017011107.2:c.2685G=	XP_016866596.1:p.Lys895=
XR_002956289.1:n.2948G=
NM_001363725.2:c.534G=	NP_001350654.1:p.Lys178=
NM_001371656.1:c.3072G=	NP_001358585.1:p.Lys1024=
NM_001374820.1:c.3072G=	NP_001361749.1:p.Lys1024=
NM_001374828.1:c.3033G= MANE Select	NP_001361757.1:p.Lys1011=
NM_017519.3:c.3033G=	NP_059989.3:p.Lys1011=