Canonical Allele Identifier: CA366242356

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522395C>A (hg19) ; chr6:g.157201261C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201261C>A , CM000668.2:g.157201261C>A	GRCh38
NC_000006.11:g.157522395C>A , CM000668.1:g.157522395C>A	GRCh37
NC_000006.10:g.157564087C>A	NCBI36
NG_032093.1:g.428332C>A
NG_032093.2:g.428332C>A
NG_066624.1:g.430236C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4877C>A	ENSP00000055163.8:p.Pro1626Gln
ENST00000414678.8:c.4946C>A	ENSP00000412835.3:p.Pro1649Gln
ENST00000637015.2:c.5165C>A	ENSP00000489729.2:p.Pro1722Gln
ENST00000346085.10:c.4916C>A	ENSP00000344546.5:p.Pro1639Gln
ENST00000350026.10:c.4628C>A	ENSP00000055163.7:p.Pro1543Gln
ENST00000414678.7:c.3194C>A	ENSP00000412835.2:p.Pro1065Gln
ENST00000635849.1:c.2357C>A	ENSP00000490948.1:p.Pro786Gln
ENST00000635957.1:c.1988C>A	ENSP00000490385.1:p.Pro663Gln
ENST00000636227.1:n.3499C>A
ENST00000636254.1:n.956C>A
ENST00000636930.2:c.5036C>A MANE Select	ENSP00000490491.2:p.Pro1679Gln
ENST00000636940.1:n.3033C>A
ENST00000637015.1:c.2404C>A
ENST00000637568.1:c.2318C>A
ENST00000637741.1:n.1702C>A
ENST00000637810.1:c.2378C>A	ENSP00000489636.1:p.Pro793Gln
ENST00000637904.1:c.2537C>A	ENSP00000490550.1:p.Pro846Gln
ENST00000647938.1:c.4667C>A	ENSP00000498155.1:p.Pro1556Gln
ENST00000346085.9:c.4667C>A	ENSP00000344546.4:p.Pro1556Gln
ENST00000350026.9:c.4628C>A	ENSP00000055163.7:p.Pro1543Gln
ENST00000414678.6:c.3194C>A	ENSP00000412835.2:p.Pro1065Gln
NM_017519.2:c.4628C>A	NP_059989.2:p.Pro1543Gln
NM_020732.3:c.4667C>A	NP_065783.3:p.Pro1556Gln
XM_005267069.3:c.4787C>A	XP_005267126.2:p.Pro1596Gln
XM_011535984.1:c.3866C>A	XP_011534286.1:p.Pro1289Gln
XM_011535985.1:c.3686C>A	XP_011534287.1:p.Pro1229Gln
XM_011535986.1:c.3446C>A	XP_011534288.1:p.Pro1149Gln
XM_011535987.1:c.3065C>A	XP_011534289.1:p.Pro1022Gln
XM_011535988.1:c.1928C>A	XP_011534290.1:p.Pro643Gln
NM_001346813.1:c.4787C>A	NP_001333742.1:p.Pro1596Gln
NM_001363725.1:c.2537C>A	NP_001350654.1:p.Pro846Gln
XM_011535984.2:c.4997C>A	XP_011534286.2:p.Pro1666Gln
XM_011535988.3:c.1928C>A	XP_011534290.1:p.Pro643Gln
XM_017011103.2:c.4898C>A	XP_016866592.1:p.Pro1633Gln
XM_017011104.1:c.4868C>A	XP_016866593.1:p.Pro1623Gln
XM_017011105.2:c.4838C>A	XP_016866594.1:p.Pro1613Gln
XM_017011106.2:c.4709C>A	XP_016866595.1:p.Pro1570Gln
XM_017011107.2:c.4688C>A	XP_016866596.1:p.Pro1563Gln
XR_002956289.1:n.4983C>A
NM_001363725.2:c.2537C>A	NP_001350654.1:p.Pro846Gln
NM_001371656.1:c.4916C>A	NP_001358585.1:p.Pro1639Gln
NM_001374820.1:c.4916C>A	NP_001361749.1:p.Pro1639Gln
NM_001374828.1:c.5036C>A MANE Select	NP_001361757.1:p.Pro1679Gln
NM_017519.3:c.4877C>A	NP_059989.3:p.Pro1626Gln