Canonical Allele Identifier: CA1675523041

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201133T= , CM000668.2:g.157201133T=	GRCh38
NC_000006.11:g.157522267T= , CM000668.1:g.157522267T=	GRCh37
NC_000006.10:g.157563959T=	NCBI36
NG_032093.1:g.428204T=
NG_032093.2:g.428204T=
NG_066624.1:g.430108T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4749T=	ENSP00000055163.8:p.Pro1583=
ENST00000414678.8:c.4818T=	ENSP00000412835.3:p.Pro1606=
ENST00000637015.2:c.5037T=	ENSP00000489729.2:p.Pro1679=
ENST00000346085.10:c.4788T=	ENSP00000344546.5:p.Pro1596=
ENST00000350026.10:c.4500T=	ENSP00000055163.7:p.Pro1500=
ENST00000414678.7:c.3066T=	ENSP00000412835.2:p.Pro1022=
ENST00000635849.1:c.2229T=	ENSP00000490948.1:p.Pro743=
ENST00000635957.1:c.1860T=	ENSP00000490385.1:p.Pro620=
ENST00000636227.1:n.3371T=
ENST00000636254.1:n.828T=
ENST00000636930.2:c.4908T= MANE Select	ENSP00000490491.2:p.Pro1636=
ENST00000636940.1:n.2905T=
ENST00000637015.1:c.2276T=
ENST00000637568.1:c.2190T=
ENST00000637741.1:n.1574T=
ENST00000637810.1:c.2250T=	ENSP00000489636.1:p.Pro750=
ENST00000637904.1:c.2409T=	ENSP00000490550.1:p.Pro803=
ENST00000647938.1:c.4539T=	ENSP00000498155.1:p.Pro1513=
ENST00000346085.9:c.4539T=	ENSP00000344546.4:p.Pro1513=
ENST00000350026.9:c.4500T=	ENSP00000055163.7:p.Pro1500=
ENST00000414678.6:c.3066T=	ENSP00000412835.2:p.Pro1022=
NM_017519.2:c.4500T=	NP_059989.2:p.Pro1500=
NM_020732.3:c.4539T=	NP_065783.3:p.Pro1513=
XM_005267069.3:c.4659T=	XP_005267126.2:p.Pro1553=
XM_011535984.1:c.3738T=	XP_011534286.1:p.Pro1246=
XM_011535985.1:c.3558T=	XP_011534287.1:p.Pro1186=
XM_011535986.1:c.3318T=	XP_011534288.1:p.Pro1106=
XM_011535987.1:c.2937T=	XP_011534289.1:p.Pro979=
XM_011535988.1:c.1800T=	XP_011534290.1:p.Pro600=
NM_001346813.1:c.4659T=	NP_001333742.1:p.Pro1553=
NM_001363725.1:c.2409T=	NP_001350654.1:p.Pro803=
XM_011535984.2:c.4869T=	XP_011534286.2:p.Pro1623=
XM_011535988.3:c.1800T=	XP_011534290.1:p.Pro600=
XM_017011103.2:c.4770T=	XP_016866592.1:p.Pro1590=
XM_017011104.1:c.4740T=	XP_016866593.1:p.Pro1580=
XM_017011105.2:c.4710T=	XP_016866594.1:p.Pro1570=
XM_017011106.2:c.4581T=	XP_016866595.1:p.Pro1527=
XM_017011107.2:c.4560T=	XP_016866596.1:p.Pro1520=
XR_002956289.1:n.4855T=
NM_001363725.2:c.2409T=	NP_001350654.1:p.Pro803=
NM_001371656.1:c.4788T=	NP_001358585.1:p.Pro1596=
NM_001374820.1:c.4788T=	NP_001361749.1:p.Pro1596=
NM_001374828.1:c.4908T= MANE Select	NP_001361757.1:p.Pro1636=
NM_017519.3:c.4749T=	NP_059989.3:p.Pro1583=