Canonical Allele Identifier: CA1675523467

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201351C= , CM000668.2:g.157201351C=	GRCh38
NC_000006.11:g.157522485C= , CM000668.1:g.157522485C=	GRCh37
NC_000006.10:g.157564177C=	NCBI36
NG_032093.1:g.428422C=
NG_032093.2:g.428422C=
NG_066624.1:g.430326C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4967C=	ENSP00000055163.8:p.Thr1656=
ENST00000414678.8:c.5036C=	ENSP00000412835.3:p.Thr1679=
ENST00000637015.2:c.5255C=	ENSP00000489729.2:p.Thr1752=
ENST00000346085.10:c.5006C=	ENSP00000344546.5:p.Thr1669=
ENST00000350026.10:c.4718C=	ENSP00000055163.7:p.Thr1573=
ENST00000414678.7:c.3284C=	ENSP00000412835.2:p.Thr1095=
ENST00000635849.1:c.2447C=	ENSP00000490948.1:p.Thr816=
ENST00000635957.1:c.2078C=	ENSP00000490385.1:p.Thr693=
ENST00000636227.1:n.3589C=
ENST00000636254.1:n.1046C=
ENST00000636930.2:c.5126C= MANE Select	ENSP00000490491.2:p.Thr1709=
ENST00000636940.1:n.3123C=
ENST00000637015.1:c.2494C=
ENST00000637568.1:c.2408C=
ENST00000637741.1:n.1792C=
ENST00000637810.1:c.2468C=	ENSP00000489636.1:p.Thr823=
ENST00000637904.1:c.2627C=	ENSP00000490550.1:p.Thr876=
ENST00000647938.1:c.4757C=	ENSP00000498155.1:p.Thr1586=
ENST00000346085.9:c.4757C=	ENSP00000344546.4:p.Thr1586=
ENST00000350026.9:c.4718C=	ENSP00000055163.7:p.Thr1573=
ENST00000414678.6:c.3284C=	ENSP00000412835.2:p.Thr1095=
NM_017519.2:c.4718C=	NP_059989.2:p.Thr1573=
NM_020732.3:c.4757C=	NP_065783.3:p.Thr1586=
XM_005267069.3:c.4877C=	XP_005267126.2:p.Thr1626=
XM_011535984.1:c.3956C=	XP_011534286.1:p.Thr1319=
XM_011535985.1:c.3776C=	XP_011534287.1:p.Thr1259=
XM_011535986.1:c.3536C=	XP_011534288.1:p.Thr1179=
XM_011535987.1:c.3155C=	XP_011534289.1:p.Thr1052=
XM_011535988.1:c.2018C=	XP_011534290.1:p.Thr673=
NM_001346813.1:c.4877C=	NP_001333742.1:p.Thr1626=
NM_001363725.1:c.2627C=	NP_001350654.1:p.Thr876=
XM_011535984.2:c.5087C=	XP_011534286.2:p.Thr1696=
XM_011535988.3:c.2018C=	XP_011534290.1:p.Thr673=
XM_017011103.2:c.4988C=	XP_016866592.1:p.Thr1663=
XM_017011104.1:c.4958C=	XP_016866593.1:p.Thr1653=
XM_017011105.2:c.4928C=	XP_016866594.1:p.Thr1643=
XM_017011106.2:c.4799C=	XP_016866595.1:p.Thr1600=
XM_017011107.2:c.4778C=	XP_016866596.1:p.Thr1593=
XR_002956289.1:n.5073C=
NM_001363725.2:c.2627C=	NP_001350654.1:p.Thr876=
NM_001371656.1:c.5006C=	NP_001358585.1:p.Thr1669=
NM_001374820.1:c.5006C=	NP_001361749.1:p.Thr1669=
NM_001374828.1:c.5126C= MANE Select	NP_001361757.1:p.Thr1709=
NM_017519.3:c.4967C=	NP_059989.3:p.Thr1656=