Canonical Allele Identifier: CA1675517036

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148837G= , CM000668.2:g.157148837G=	GRCh38
NC_000006.11:g.157469971G= , CM000668.1:g.157469971G=	GRCh37
NC_000006.10:g.157511663G=	NCBI36
NG_032093.1:g.375908G=
NG_032093.2:g.375908G=
NG_066624.1:g.377812G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2975G=	ENSP00000055163.8:p.Gly992=
ENST00000414678.8:c.2885G=	ENSP00000412835.3:p.Gly962=
ENST00000637015.2:c.2975G=	ENSP00000489729.2:p.Gly992=
ENST00000319584.11:c.989G=	ENSP00000313006.7:p.Gly330=
ENST00000346085.10:c.3014G=	ENSP00000344546.5:p.Gly1005=
ENST00000350026.10:c.2726G=	ENSP00000055163.7:p.Gly909=
ENST00000414678.7:c.1133G=	ENSP00000412835.2:p.Gly378=
ENST00000452544.2:n.876G=
ENST00000635849.1:c.296G=	ENSP00000490948.1:p.Gly99=
ENST00000636426.1:n.109G=
ENST00000636930.2:c.2975G= MANE Select	ENSP00000490491.2:p.Gly992=
ENST00000637015.1:c.214G=
ENST00000637568.1:c.18G=
ENST00000637810.1:c.476G=	ENSP00000489636.1:p.Gly159=
ENST00000637904.1:c.476G=	ENSP00000490550.1:p.Gly159=
ENST00000647938.1:c.2765G=	ENSP00000498155.1:p.Gly922=
ENST00000674190.1:n.1724G=
ENST00000319584.10:c.992G=	ENSP00000313006.6:p.Gly331=
ENST00000346085.9:c.2765G=	ENSP00000344546.4:p.Gly922=
ENST00000350026.9:c.2726G=	ENSP00000055163.7:p.Gly909=
ENST00000414678.6:c.1133G=	ENSP00000412835.2:p.Gly378=
ENST00000452544.1:n.822G=
ENST00000478761.3:c.48G=
NM_017519.2:c.2726G=	NP_059989.2:p.Gly909=
NM_020732.3:c.2765G=	NP_065783.3:p.Gly922=
XM_005267069.3:c.2726G=	XP_005267126.2:p.Gly909=
XM_011535984.1:c.1676G=	XP_011534286.1:p.Gly559=
XM_011535985.1:c.1496G=	XP_011534287.1:p.Gly499=
XM_011535986.1:c.1256G=	XP_011534288.1:p.Gly419=
XM_011535987.1:c.875G=	XP_011534289.1:p.Gly292=
XM_011535988.1:c.-20+15630G=	XP_011534290.1:n.-20+15630G=
NM_001346813.1:c.2726G=	NP_001333742.1:p.Gly909=
NM_001363725.1:c.476G=	NP_001350654.1:p.Gly159=
XM_011535984.2:c.2807G=	XP_011534286.2:p.Gly936=
XM_011535988.3:c.-20+15630G=	XP_011534290.1:n.-20+15630G=
XM_017011103.2:c.2807G=	XP_016866592.1:p.Gly936=
XM_017011104.1:c.2807G=	XP_016866593.1:p.Gly936=
XM_017011105.2:c.2807G=	XP_016866594.1:p.Gly936=
XM_017011106.2:c.2807G=	XP_016866595.1:p.Gly936=
XM_017011107.2:c.2627G=	XP_016866596.1:p.Gly876=
XR_002956289.1:n.2890G=
NM_001363725.2:c.476G=	NP_001350654.1:p.Gly159=
NM_001371656.1:c.3014G=	NP_001358585.1:p.Gly1005=
NM_001374820.1:c.3014G=	NP_001361749.1:p.Gly1005=
NM_001374828.1:c.2975G= MANE Select	NP_001361757.1:p.Gly992=
NM_017519.3:c.2975G=	NP_059989.3:p.Gly992=