Canonical Allele Identifier: CA366241330

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522101A>T (hg19) ; chr6:g.157200967A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200967A>T , CM000668.2:g.157200967A>T	GRCh38
NC_000006.11:g.157522101A>T , CM000668.1:g.157522101A>T	GRCh37
NC_000006.10:g.157563793A>T	NCBI36
NG_032093.1:g.428038A>T
NG_032093.2:g.428038A>T
NG_066624.1:g.429942A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4583A>T	ENSP00000055163.8:p.Glu1528Val
ENST00000414678.8:c.4652A>T	ENSP00000412835.3:p.Glu1551Val
ENST00000637015.2:c.4871A>T	ENSP00000489729.2:p.Glu1624Val
ENST00000346085.10:c.4622A>T	ENSP00000344546.5:p.Glu1541Val
ENST00000350026.10:c.4334A>T	ENSP00000055163.7:p.Glu1445Val
ENST00000414678.7:c.2900A>T	ENSP00000412835.2:p.Glu967Val
ENST00000635849.1:c.2063A>T	ENSP00000490948.1:p.Glu688Val
ENST00000635957.1:c.1694A>T	ENSP00000490385.1:p.Glu565Val
ENST00000636227.1:n.3205A>T
ENST00000636254.1:n.662A>T
ENST00000636930.2:c.4742A>T MANE Select	ENSP00000490491.2:p.Glu1581Val
ENST00000636940.1:n.2739A>T
ENST00000637015.1:c.2110A>T
ENST00000637568.1:c.2024A>T
ENST00000637741.1:n.1408A>T
ENST00000637810.1:c.2084A>T	ENSP00000489636.1:p.Glu695Val
ENST00000637904.1:c.2243A>T	ENSP00000490550.1:p.Glu748Val
ENST00000647938.1:c.4373A>T	ENSP00000498155.1:p.Glu1458Val
ENST00000346085.9:c.4373A>T	ENSP00000344546.4:p.Glu1458Val
ENST00000350026.9:c.4334A>T	ENSP00000055163.7:p.Glu1445Val
ENST00000414678.6:c.2900A>T	ENSP00000412835.2:p.Glu967Val
NM_017519.2:c.4334A>T	NP_059989.2:p.Glu1445Val
NM_020732.3:c.4373A>T	NP_065783.3:p.Glu1458Val
XM_005267069.3:c.4493A>T	XP_005267126.2:p.Glu1498Val
XM_011535984.1:c.3572A>T	XP_011534286.1:p.Glu1191Val
XM_011535985.1:c.3392A>T	XP_011534287.1:p.Glu1131Val
XM_011535986.1:c.3152A>T	XP_011534288.1:p.Glu1051Val
XM_011535987.1:c.2771A>T	XP_011534289.1:p.Glu924Val
XM_011535988.1:c.1634A>T	XP_011534290.1:p.Glu545Val
NM_001346813.1:c.4493A>T	NP_001333742.1:p.Glu1498Val
NM_001363725.1:c.2243A>T	NP_001350654.1:p.Glu748Val
XM_011535984.2:c.4703A>T	XP_011534286.2:p.Glu1568Val
XM_011535988.3:c.1634A>T	XP_011534290.1:p.Glu545Val
XM_017011103.2:c.4604A>T	XP_016866592.1:p.Glu1535Val
XM_017011104.1:c.4574A>T	XP_016866593.1:p.Glu1525Val
XM_017011105.2:c.4544A>T	XP_016866594.1:p.Glu1515Val
XM_017011106.2:c.4415A>T	XP_016866595.1:p.Glu1472Val
XM_017011107.2:c.4394A>T	XP_016866596.1:p.Glu1465Val
XR_002956289.1:n.4689A>T
NM_001363725.2:c.2243A>T	NP_001350654.1:p.Glu748Val
NM_001371656.1:c.4622A>T	NP_001358585.1:p.Glu1541Val
NM_001374820.1:c.4622A>T	NP_001361749.1:p.Glu1541Val
NM_001374828.1:c.4742A>T MANE Select	NP_001361757.1:p.Glu1581Val
NM_017519.3:c.4583A>T	NP_059989.3:p.Glu1528Val