Canonical Allele Identifier: CA452978142

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522312C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201178C>A , CM000668.2:g.157201178C>A	GRCh38
NC_000006.11:g.157522312C>A , CM000668.1:g.157522312C>A	GRCh37
NC_000006.10:g.157564004C>A	NCBI36
NG_032093.1:g.428249C>A
NG_032093.2:g.428249C>A
NG_066624.1:g.430153C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4794C>A	ENSP00000055163.8:p.Ser1598=
ENST00000414678.8:c.4863C>A	ENSP00000412835.3:p.Ser1621=
ENST00000637015.2:c.5082C>A	ENSP00000489729.2:p.Ser1694=
ENST00000346085.10:c.4833C>A	ENSP00000344546.5:p.Ser1611=
ENST00000350026.10:c.4545C>A	ENSP00000055163.7:p.Ser1515=
ENST00000414678.7:c.3111C>A	ENSP00000412835.2:p.Ser1037=
ENST00000635849.1:c.2274C>A	ENSP00000490948.1:p.Ser758=
ENST00000635957.1:c.1905C>A	ENSP00000490385.1:p.Ser635=
ENST00000636227.1:n.3416C>A
ENST00000636254.1:n.873C>A
ENST00000636930.2:c.4953C>A MANE Select	ENSP00000490491.2:p.Ser1651=
ENST00000636940.1:n.2950C>A
ENST00000637015.1:c.2321C>A
ENST00000637568.1:c.2235C>A
ENST00000637741.1:n.1619C>A
ENST00000637810.1:c.2295C>A	ENSP00000489636.1:p.Ser765=
ENST00000637904.1:c.2454C>A	ENSP00000490550.1:p.Ser818=
ENST00000647938.1:c.4584C>A	ENSP00000498155.1:p.Ser1528=
ENST00000346085.9:c.4584C>A	ENSP00000344546.4:p.Ser1528=
ENST00000350026.9:c.4545C>A	ENSP00000055163.7:p.Ser1515=
ENST00000414678.6:c.3111C>A	ENSP00000412835.2:p.Ser1037=
NM_017519.2:c.4545C>A	NP_059989.2:p.Ser1515=
NM_020732.3:c.4584C>A	NP_065783.3:p.Ser1528=
XM_005267069.3:c.4704C>A	XP_005267126.2:p.Ser1568=
XM_011535984.1:c.3783C>A	XP_011534286.1:p.Ser1261=
XM_011535985.1:c.3603C>A	XP_011534287.1:p.Ser1201=
XM_011535986.1:c.3363C>A	XP_011534288.1:p.Ser1121=
XM_011535987.1:c.2982C>A	XP_011534289.1:p.Ser994=
XM_011535988.1:c.1845C>A	XP_011534290.1:p.Ser615=
NM_001346813.1:c.4704C>A	NP_001333742.1:p.Ser1568=
NM_001363725.1:c.2454C>A	NP_001350654.1:p.Ser818=
XM_011535984.2:c.4914C>A	XP_011534286.2:p.Ser1638=
XM_011535988.3:c.1845C>A	XP_011534290.1:p.Ser615=
XM_017011103.2:c.4815C>A	XP_016866592.1:p.Ser1605=
XM_017011104.1:c.4785C>A	XP_016866593.1:p.Ser1595=
XM_017011105.2:c.4755C>A	XP_016866594.1:p.Ser1585=
XM_017011106.2:c.4626C>A	XP_016866595.1:p.Ser1542=
XM_017011107.2:c.4605C>A	XP_016866596.1:p.Ser1535=
XR_002956289.1:n.4900C>A
NM_001363725.2:c.2454C>A	NP_001350654.1:p.Ser818=
NM_001371656.1:c.4833C>A	NP_001358585.1:p.Ser1611=
NM_001374820.1:c.4833C>A	NP_001361749.1:p.Ser1611=
NM_001374828.1:c.4953C>A MANE Select	NP_001361757.1:p.Ser1651=
NM_017519.3:c.4794C>A	NP_059989.3:p.Ser1598=