Canonical Allele Identifier: CA366241634

Gene: ARID1B

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4652C>A	ENSP00000055163.8:p.Pro1551His
ENST00000414678.8:c.4721C>A	ENSP00000412835.3:p.Pro1574His
ENST00000637015.2:c.4940C>A	ENSP00000489729.2:p.Pro1647His
ENST00000346085.10:c.4691C>A	ENSP00000344546.5:p.Pro1564His
ENST00000350026.10:c.4403C>A	ENSP00000055163.7:p.Pro1468His
ENST00000414678.7:c.2969C>A	ENSP00000412835.2:p.Pro990His
ENST00000635849.1:c.2132C>A	ENSP00000490948.1:p.Pro711His
ENST00000635957.1:c.1763C>A	ENSP00000490385.1:p.Pro588His
ENST00000636227.1:n.3274C>A
ENST00000636254.1:n.731C>A
ENST00000636930.2:c.4811C>A MANE Select	ENSP00000490491.2:p.Pro1604His
ENST00000636940.1:n.2808C>A
ENST00000637015.1:c.2179C>A
ENST00000637568.1:c.2093C>A
ENST00000637741.1:n.1477C>A
ENST00000637810.1:c.2153C>A	ENSP00000489636.1:p.Pro718His
ENST00000637904.1:c.2312C>A	ENSP00000490550.1:p.Pro771His
ENST00000647938.1:c.4442C>A	ENSP00000498155.1:p.Pro1481His
ENST00000346085.9:c.4442C>A	ENSP00000344546.4:p.Pro1481His
ENST00000350026.9:c.4403C>A	ENSP00000055163.7:p.Pro1468His
ENST00000414678.6:c.2969C>A	ENSP00000412835.2:p.Pro990His
NM_017519.2:c.4403C>A	NP_059989.2:p.Pro1468His
NM_020732.3:c.4442C>A	NP_065783.3:p.Pro1481His
XM_005267069.3:c.4562C>A	XP_005267126.2:p.Pro1521His
XM_011535984.1:c.3641C>A	XP_011534286.1:p.Pro1214His
XM_011535985.1:c.3461C>A	XP_011534287.1:p.Pro1154His
XM_011535986.1:c.3221C>A	XP_011534288.1:p.Pro1074His
XM_011535987.1:c.2840C>A	XP_011534289.1:p.Pro947His
XM_011535988.1:c.1703C>A	XP_011534290.1:p.Pro568His
NM_001346813.1:c.4562C>A	NP_001333742.1:p.Pro1521His
NM_001363725.1:c.2312C>A	NP_001350654.1:p.Pro771His
XM_011535984.2:c.4772C>A	XP_011534286.2:p.Pro1591His
XM_011535988.3:c.1703C>A	XP_011534290.1:p.Pro568His
XM_017011103.2:c.4673C>A	XP_016866592.1:p.Pro1558His
XM_017011104.1:c.4643C>A	XP_016866593.1:p.Pro1548His
XM_017011105.2:c.4613C>A	XP_016866594.1:p.Pro1538His
XM_017011106.2:c.4484C>A	XP_016866595.1:p.Pro1495His
XM_017011107.2:c.4463C>A	XP_016866596.1:p.Pro1488His
XR_002956289.1:n.4758C>A
NM_001363725.2:c.2312C>A	NP_001350654.1:p.Pro771His
NM_001371656.1:c.4691C>A	NP_001358585.1:p.Pro1564His
NM_001374820.1:c.4691C>A	NP_001361749.1:p.Pro1564His
NM_001374828.1:c.4811C>A MANE Select	NP_001361757.1:p.Pro1604His
NM_017519.3:c.4652C>A	NP_059989.3:p.Pro1551His