Canonical Allele Identifier: CA366242082

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522269C>A (hg19) ; chr6:g.157201135C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201135C>A , CM000668.2:g.157201135C>A	GRCh38
NC_000006.11:g.157522269C>A , CM000668.1:g.157522269C>A	GRCh37
NC_000006.10:g.157563961C>A	NCBI36
NG_032093.1:g.428206C>A
NG_032093.2:g.428206C>A
NG_066624.1:g.430110C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4751C>A	ENSP00000055163.8:p.Ser1584Tyr
ENST00000414678.8:c.4820C>A	ENSP00000412835.3:p.Ser1607Tyr
ENST00000637015.2:c.5039C>A	ENSP00000489729.2:p.Ser1680Tyr
ENST00000346085.10:c.4790C>A	ENSP00000344546.5:p.Ser1597Tyr
ENST00000350026.10:c.4502C>A	ENSP00000055163.7:p.Ser1501Tyr
ENST00000414678.7:c.3068C>A	ENSP00000412835.2:p.Ser1023Tyr
ENST00000635849.1:c.2231C>A	ENSP00000490948.1:p.Ser744Tyr
ENST00000635957.1:c.1862C>A	ENSP00000490385.1:p.Ser621Tyr
ENST00000636227.1:n.3373C>A
ENST00000636254.1:n.830C>A
ENST00000636930.2:c.4910C>A MANE Select	ENSP00000490491.2:p.Ser1637Tyr
ENST00000636940.1:n.2907C>A
ENST00000637015.1:c.2278C>A
ENST00000637568.1:c.2192C>A
ENST00000637741.1:n.1576C>A
ENST00000637810.1:c.2252C>A	ENSP00000489636.1:p.Ser751Tyr
ENST00000637904.1:c.2411C>A	ENSP00000490550.1:p.Ser804Tyr
ENST00000647938.1:c.4541C>A	ENSP00000498155.1:p.Ser1514Tyr
ENST00000346085.9:c.4541C>A	ENSP00000344546.4:p.Ser1514Tyr
ENST00000350026.9:c.4502C>A	ENSP00000055163.7:p.Ser1501Tyr
ENST00000414678.6:c.3068C>A	ENSP00000412835.2:p.Ser1023Tyr
NM_017519.2:c.4502C>A	NP_059989.2:p.Ser1501Tyr
NM_020732.3:c.4541C>A	NP_065783.3:p.Ser1514Tyr
XM_005267069.3:c.4661C>A	XP_005267126.2:p.Ser1554Tyr
XM_011535984.1:c.3740C>A	XP_011534286.1:p.Ser1247Tyr
XM_011535985.1:c.3560C>A	XP_011534287.1:p.Ser1187Tyr
XM_011535986.1:c.3320C>A	XP_011534288.1:p.Ser1107Tyr
XM_011535987.1:c.2939C>A	XP_011534289.1:p.Ser980Tyr
XM_011535988.1:c.1802C>A	XP_011534290.1:p.Ser601Tyr
NM_001346813.1:c.4661C>A	NP_001333742.1:p.Ser1554Tyr
NM_001363725.1:c.2411C>A	NP_001350654.1:p.Ser804Tyr
XM_011535984.2:c.4871C>A	XP_011534286.2:p.Ser1624Tyr
XM_011535988.3:c.1802C>A	XP_011534290.1:p.Ser601Tyr
XM_017011103.2:c.4772C>A	XP_016866592.1:p.Ser1591Tyr
XM_017011104.1:c.4742C>A	XP_016866593.1:p.Ser1581Tyr
XM_017011105.2:c.4712C>A	XP_016866594.1:p.Ser1571Tyr
XM_017011106.2:c.4583C>A	XP_016866595.1:p.Ser1528Tyr
XM_017011107.2:c.4562C>A	XP_016866596.1:p.Ser1521Tyr
XR_002956289.1:n.4857C>A
NM_001363725.2:c.2411C>A	NP_001350654.1:p.Ser804Tyr
NM_001371656.1:c.4790C>A	NP_001358585.1:p.Ser1597Tyr
NM_001374820.1:c.4790C>A	NP_001361749.1:p.Ser1597Tyr
NM_001374828.1:c.4910C>A MANE Select	NP_001361757.1:p.Ser1637Tyr
NM_017519.3:c.4751C>A	NP_059989.3:p.Ser1584Tyr