Canonical Allele Identifier: CA366242076

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522266C>G (hg19) ; chr6:g.157201132C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201132C>G , CM000668.2:g.157201132C>G	GRCh38
NC_000006.11:g.157522266C>G , CM000668.1:g.157522266C>G	GRCh37
NC_000006.10:g.157563958C>G	NCBI36
NG_032093.1:g.428203C>G
NG_032093.2:g.428203C>G
NG_066624.1:g.430107C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4748C>G	ENSP00000055163.8:p.Pro1583Arg
ENST00000414678.8:c.4817C>G	ENSP00000412835.3:p.Pro1606Arg
ENST00000637015.2:c.5036C>G	ENSP00000489729.2:p.Pro1679Arg
ENST00000346085.10:c.4787C>G	ENSP00000344546.5:p.Pro1596Arg
ENST00000350026.10:c.4499C>G	ENSP00000055163.7:p.Pro1500Arg
ENST00000414678.7:c.3065C>G	ENSP00000412835.2:p.Pro1022Arg
ENST00000635849.1:c.2228C>G	ENSP00000490948.1:p.Pro743Arg
ENST00000635957.1:c.1859C>G	ENSP00000490385.1:p.Pro620Arg
ENST00000636227.1:n.3370C>G
ENST00000636254.1:n.827C>G
ENST00000636930.2:c.4907C>G MANE Select	ENSP00000490491.2:p.Pro1636Arg
ENST00000636940.1:n.2904C>G
ENST00000637015.1:c.2275C>G
ENST00000637568.1:c.2189C>G
ENST00000637741.1:n.1573C>G
ENST00000637810.1:c.2249C>G	ENSP00000489636.1:p.Pro750Arg
ENST00000637904.1:c.2408C>G	ENSP00000490550.1:p.Pro803Arg
ENST00000647938.1:c.4538C>G	ENSP00000498155.1:p.Pro1513Arg
ENST00000346085.9:c.4538C>G	ENSP00000344546.4:p.Pro1513Arg
ENST00000350026.9:c.4499C>G	ENSP00000055163.7:p.Pro1500Arg
ENST00000414678.6:c.3065C>G	ENSP00000412835.2:p.Pro1022Arg
NM_017519.2:c.4499C>G	NP_059989.2:p.Pro1500Arg
NM_020732.3:c.4538C>G	NP_065783.3:p.Pro1513Arg
XM_005267069.3:c.4658C>G	XP_005267126.2:p.Pro1553Arg
XM_011535984.1:c.3737C>G	XP_011534286.1:p.Pro1246Arg
XM_011535985.1:c.3557C>G	XP_011534287.1:p.Pro1186Arg
XM_011535986.1:c.3317C>G	XP_011534288.1:p.Pro1106Arg
XM_011535987.1:c.2936C>G	XP_011534289.1:p.Pro979Arg
XM_011535988.1:c.1799C>G	XP_011534290.1:p.Pro600Arg
NM_001346813.1:c.4658C>G	NP_001333742.1:p.Pro1553Arg
NM_001363725.1:c.2408C>G	NP_001350654.1:p.Pro803Arg
XM_011535984.2:c.4868C>G	XP_011534286.2:p.Pro1623Arg
XM_011535988.3:c.1799C>G	XP_011534290.1:p.Pro600Arg
XM_017011103.2:c.4769C>G	XP_016866592.1:p.Pro1590Arg
XM_017011104.1:c.4739C>G	XP_016866593.1:p.Pro1580Arg
XM_017011105.2:c.4709C>G	XP_016866594.1:p.Pro1570Arg
XM_017011106.2:c.4580C>G	XP_016866595.1:p.Pro1527Arg
XM_017011107.2:c.4559C>G	XP_016866596.1:p.Pro1520Arg
XR_002956289.1:n.4854C>G
NM_001363725.2:c.2408C>G	NP_001350654.1:p.Pro803Arg
NM_001371656.1:c.4787C>G	NP_001358585.1:p.Pro1596Arg
NM_001374820.1:c.4787C>G	NP_001361749.1:p.Pro1596Arg
NM_001374828.1:c.4907C>G MANE Select	NP_001361757.1:p.Pro1636Arg
NM_017519.3:c.4748C>G	NP_059989.3:p.Pro1583Arg