Canonical Allele Identifier: CA366242083

Gene: ARID1B

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4751C>G	ENSP00000055163.8:p.Ser1584Cys
ENST00000414678.8:c.4820C>G	ENSP00000412835.3:p.Ser1607Cys
ENST00000637015.2:c.5039C>G	ENSP00000489729.2:p.Ser1680Cys
ENST00000346085.10:c.4790C>G	ENSP00000344546.5:p.Ser1597Cys
ENST00000350026.10:c.4502C>G	ENSP00000055163.7:p.Ser1501Cys
ENST00000414678.7:c.3068C>G	ENSP00000412835.2:p.Ser1023Cys
ENST00000635849.1:c.2231C>G	ENSP00000490948.1:p.Ser744Cys
ENST00000635957.1:c.1862C>G	ENSP00000490385.1:p.Ser621Cys
ENST00000636227.1:n.3373C>G
ENST00000636254.1:n.830C>G
ENST00000636930.2:c.4910C>G MANE Select	ENSP00000490491.2:p.Ser1637Cys
ENST00000636940.1:n.2907C>G
ENST00000637015.1:c.2278C>G
ENST00000637568.1:c.2192C>G
ENST00000637741.1:n.1576C>G
ENST00000637810.1:c.2252C>G	ENSP00000489636.1:p.Ser751Cys
ENST00000637904.1:c.2411C>G	ENSP00000490550.1:p.Ser804Cys
ENST00000647938.1:c.4541C>G	ENSP00000498155.1:p.Ser1514Cys
ENST00000346085.9:c.4541C>G	ENSP00000344546.4:p.Ser1514Cys
ENST00000350026.9:c.4502C>G	ENSP00000055163.7:p.Ser1501Cys
ENST00000414678.6:c.3068C>G	ENSP00000412835.2:p.Ser1023Cys
NM_017519.2:c.4502C>G	NP_059989.2:p.Ser1501Cys
NM_020732.3:c.4541C>G	NP_065783.3:p.Ser1514Cys
XM_005267069.3:c.4661C>G	XP_005267126.2:p.Ser1554Cys
XM_011535984.1:c.3740C>G	XP_011534286.1:p.Ser1247Cys
XM_011535985.1:c.3560C>G	XP_011534287.1:p.Ser1187Cys
XM_011535986.1:c.3320C>G	XP_011534288.1:p.Ser1107Cys
XM_011535987.1:c.2939C>G	XP_011534289.1:p.Ser980Cys
XM_011535988.1:c.1802C>G	XP_011534290.1:p.Ser601Cys
NM_001346813.1:c.4661C>G	NP_001333742.1:p.Ser1554Cys
NM_001363725.1:c.2411C>G	NP_001350654.1:p.Ser804Cys
XM_011535984.2:c.4871C>G	XP_011534286.2:p.Ser1624Cys
XM_011535988.3:c.1802C>G	XP_011534290.1:p.Ser601Cys
XM_017011103.2:c.4772C>G	XP_016866592.1:p.Ser1591Cys
XM_017011104.1:c.4742C>G	XP_016866593.1:p.Ser1581Cys
XM_017011105.2:c.4712C>G	XP_016866594.1:p.Ser1571Cys
XM_017011106.2:c.4583C>G	XP_016866595.1:p.Ser1528Cys
XM_017011107.2:c.4562C>G	XP_016866596.1:p.Ser1521Cys
XR_002956289.1:n.4857C>G
NM_001363725.2:c.2411C>G	NP_001350654.1:p.Ser804Cys
NM_001371656.1:c.4790C>G	NP_001358585.1:p.Ser1597Cys
NM_001374820.1:c.4790C>G	NP_001361749.1:p.Ser1597Cys
NM_001374828.1:c.4910C>G MANE Select	NP_001361757.1:p.Ser1637Cys
NM_017519.3:c.4751C>G	NP_059989.3:p.Ser1584Cys