Canonical Allele Identifier: CA452978273

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522414C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201280C>A , CM000668.2:g.157201280C>A	GRCh38
NC_000006.11:g.157522414C>A , CM000668.1:g.157522414C>A	GRCh37
NC_000006.10:g.157564106C>A	NCBI36
NG_032093.1:g.428351C>A
NG_032093.2:g.428351C>A
NG_066624.1:g.430255C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4896C>A	ENSP00000055163.8:p.Ser1632=
ENST00000414678.8:c.4965C>A	ENSP00000412835.3:p.Ser1655=
ENST00000637015.2:c.5184C>A	ENSP00000489729.2:p.Ser1728=
ENST00000346085.10:c.4935C>A	ENSP00000344546.5:p.Ser1645=
ENST00000350026.10:c.4647C>A	ENSP00000055163.7:p.Ser1549=
ENST00000414678.7:c.3213C>A	ENSP00000412835.2:p.Ser1071=
ENST00000635849.1:c.2376C>A	ENSP00000490948.1:p.Ser792=
ENST00000635957.1:c.2007C>A	ENSP00000490385.1:p.Ser669=
ENST00000636227.1:n.3518C>A
ENST00000636254.1:n.975C>A
ENST00000636930.2:c.5055C>A MANE Select	ENSP00000490491.2:p.Ser1685=
ENST00000636940.1:n.3052C>A
ENST00000637015.1:c.2423C>A
ENST00000637568.1:c.2337C>A
ENST00000637741.1:n.1721C>A
ENST00000637810.1:c.2397C>A	ENSP00000489636.1:p.Ser799=
ENST00000637904.1:c.2556C>A	ENSP00000490550.1:p.Ser852=
ENST00000647938.1:c.4686C>A	ENSP00000498155.1:p.Ser1562=
ENST00000346085.9:c.4686C>A	ENSP00000344546.4:p.Ser1562=
ENST00000350026.9:c.4647C>A	ENSP00000055163.7:p.Ser1549=
ENST00000414678.6:c.3213C>A	ENSP00000412835.2:p.Ser1071=
NM_017519.2:c.4647C>A	NP_059989.2:p.Ser1549=
NM_020732.3:c.4686C>A	NP_065783.3:p.Ser1562=
XM_005267069.3:c.4806C>A	XP_005267126.2:p.Ser1602=
XM_011535984.1:c.3885C>A	XP_011534286.1:p.Ser1295=
XM_011535985.1:c.3705C>A	XP_011534287.1:p.Ser1235=
XM_011535986.1:c.3465C>A	XP_011534288.1:p.Ser1155=
XM_011535987.1:c.3084C>A	XP_011534289.1:p.Ser1028=
XM_011535988.1:c.1947C>A	XP_011534290.1:p.Ser649=
NM_001346813.1:c.4806C>A	NP_001333742.1:p.Ser1602=
NM_001363725.1:c.2556C>A	NP_001350654.1:p.Ser852=
XM_011535984.2:c.5016C>A	XP_011534286.2:p.Ser1672=
XM_011535988.3:c.1947C>A	XP_011534290.1:p.Ser649=
XM_017011103.2:c.4917C>A	XP_016866592.1:p.Ser1639=
XM_017011104.1:c.4887C>A	XP_016866593.1:p.Ser1629=
XM_017011105.2:c.4857C>A	XP_016866594.1:p.Ser1619=
XM_017011106.2:c.4728C>A	XP_016866595.1:p.Ser1576=
XM_017011107.2:c.4707C>A	XP_016866596.1:p.Ser1569=
XR_002956289.1:n.5002C>A
NM_001363725.2:c.2556C>A	NP_001350654.1:p.Ser852=
NM_001371656.1:c.4935C>A	NP_001358585.1:p.Ser1645=
NM_001374820.1:c.4935C>A	NP_001361749.1:p.Ser1645=
NM_001374828.1:c.5055C>A MANE Select	NP_001361757.1:p.Ser1685=
NM_017519.3:c.4896C>A	NP_059989.3:p.Ser1632=