Canonical Allele Identifier: CA366241636

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522170C>G (hg19) ; chr6:g.157201036C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201036C>G , CM000668.2:g.157201036C>G	GRCh38
NC_000006.11:g.157522170C>G , CM000668.1:g.157522170C>G	GRCh37
NC_000006.10:g.157563862C>G	NCBI36
NG_032093.1:g.428107C>G
NG_032093.2:g.428107C>G
NG_066624.1:g.430011C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4652C>G	ENSP00000055163.8:p.Pro1551Arg
ENST00000414678.8:c.4721C>G	ENSP00000412835.3:p.Pro1574Arg
ENST00000637015.2:c.4940C>G	ENSP00000489729.2:p.Pro1647Arg
ENST00000346085.10:c.4691C>G	ENSP00000344546.5:p.Pro1564Arg
ENST00000350026.10:c.4403C>G	ENSP00000055163.7:p.Pro1468Arg
ENST00000414678.7:c.2969C>G	ENSP00000412835.2:p.Pro990Arg
ENST00000635849.1:c.2132C>G	ENSP00000490948.1:p.Pro711Arg
ENST00000635957.1:c.1763C>G	ENSP00000490385.1:p.Pro588Arg
ENST00000636227.1:n.3274C>G
ENST00000636254.1:n.731C>G
ENST00000636930.2:c.4811C>G MANE Select	ENSP00000490491.2:p.Pro1604Arg
ENST00000636940.1:n.2808C>G
ENST00000637015.1:c.2179C>G
ENST00000637568.1:c.2093C>G
ENST00000637741.1:n.1477C>G
ENST00000637810.1:c.2153C>G	ENSP00000489636.1:p.Pro718Arg
ENST00000637904.1:c.2312C>G	ENSP00000490550.1:p.Pro771Arg
ENST00000647938.1:c.4442C>G	ENSP00000498155.1:p.Pro1481Arg
ENST00000346085.9:c.4442C>G	ENSP00000344546.4:p.Pro1481Arg
ENST00000350026.9:c.4403C>G	ENSP00000055163.7:p.Pro1468Arg
ENST00000414678.6:c.2969C>G	ENSP00000412835.2:p.Pro990Arg
NM_017519.2:c.4403C>G	NP_059989.2:p.Pro1468Arg
NM_020732.3:c.4442C>G	NP_065783.3:p.Pro1481Arg
XM_005267069.3:c.4562C>G	XP_005267126.2:p.Pro1521Arg
XM_011535984.1:c.3641C>G	XP_011534286.1:p.Pro1214Arg
XM_011535985.1:c.3461C>G	XP_011534287.1:p.Pro1154Arg
XM_011535986.1:c.3221C>G	XP_011534288.1:p.Pro1074Arg
XM_011535987.1:c.2840C>G	XP_011534289.1:p.Pro947Arg
XM_011535988.1:c.1703C>G	XP_011534290.1:p.Pro568Arg
NM_001346813.1:c.4562C>G	NP_001333742.1:p.Pro1521Arg
NM_001363725.1:c.2312C>G	NP_001350654.1:p.Pro771Arg
XM_011535984.2:c.4772C>G	XP_011534286.2:p.Pro1591Arg
XM_011535988.3:c.1703C>G	XP_011534290.1:p.Pro568Arg
XM_017011103.2:c.4673C>G	XP_016866592.1:p.Pro1558Arg
XM_017011104.1:c.4643C>G	XP_016866593.1:p.Pro1548Arg
XM_017011105.2:c.4613C>G	XP_016866594.1:p.Pro1538Arg
XM_017011106.2:c.4484C>G	XP_016866595.1:p.Pro1495Arg
XM_017011107.2:c.4463C>G	XP_016866596.1:p.Pro1488Arg
XR_002956289.1:n.4758C>G
NM_001363725.2:c.2312C>G	NP_001350654.1:p.Pro771Arg
NM_001371656.1:c.4691C>G	NP_001358585.1:p.Pro1564Arg
NM_001374820.1:c.4691C>G	NP_001361749.1:p.Pro1564Arg
NM_001374828.1:c.4811C>G MANE Select	NP_001361757.1:p.Pro1604Arg
NM_017519.3:c.4652C>G	NP_059989.3:p.Pro1551Arg