Canonical Allele Identifier: CA366242393

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522413C>A (hg19) ; chr6:g.157201279C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201279C>A , CM000668.2:g.157201279C>A	GRCh38
NC_000006.11:g.157522413C>A , CM000668.1:g.157522413C>A	GRCh37
NC_000006.10:g.157564105C>A	NCBI36
NG_032093.1:g.428350C>A
NG_032093.2:g.428350C>A
NG_066624.1:g.430254C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4895C>A	ENSP00000055163.8:p.Ser1632Tyr
ENST00000414678.8:c.4964C>A	ENSP00000412835.3:p.Ser1655Tyr
ENST00000637015.2:c.5183C>A	ENSP00000489729.2:p.Ser1728Tyr
ENST00000346085.10:c.4934C>A	ENSP00000344546.5:p.Ser1645Tyr
ENST00000350026.10:c.4646C>A	ENSP00000055163.7:p.Ser1549Tyr
ENST00000414678.7:c.3212C>A	ENSP00000412835.2:p.Ser1071Tyr
ENST00000635849.1:c.2375C>A	ENSP00000490948.1:p.Ser792Tyr
ENST00000635957.1:c.2006C>A	ENSP00000490385.1:p.Ser669Tyr
ENST00000636227.1:n.3517C>A
ENST00000636254.1:n.974C>A
ENST00000636930.2:c.5054C>A MANE Select	ENSP00000490491.2:p.Ser1685Tyr
ENST00000636940.1:n.3051C>A
ENST00000637015.1:c.2422C>A
ENST00000637568.1:c.2336C>A
ENST00000637741.1:n.1720C>A
ENST00000637810.1:c.2396C>A	ENSP00000489636.1:p.Ser799Tyr
ENST00000637904.1:c.2555C>A	ENSP00000490550.1:p.Ser852Tyr
ENST00000647938.1:c.4685C>A	ENSP00000498155.1:p.Ser1562Tyr
ENST00000346085.9:c.4685C>A	ENSP00000344546.4:p.Ser1562Tyr
ENST00000350026.9:c.4646C>A	ENSP00000055163.7:p.Ser1549Tyr
ENST00000414678.6:c.3212C>A	ENSP00000412835.2:p.Ser1071Tyr
NM_017519.2:c.4646C>A	NP_059989.2:p.Ser1549Tyr
NM_020732.3:c.4685C>A	NP_065783.3:p.Ser1562Tyr
XM_005267069.3:c.4805C>A	XP_005267126.2:p.Ser1602Tyr
XM_011535984.1:c.3884C>A	XP_011534286.1:p.Ser1295Tyr
XM_011535985.1:c.3704C>A	XP_011534287.1:p.Ser1235Tyr
XM_011535986.1:c.3464C>A	XP_011534288.1:p.Ser1155Tyr
XM_011535987.1:c.3083C>A	XP_011534289.1:p.Ser1028Tyr
XM_011535988.1:c.1946C>A	XP_011534290.1:p.Ser649Tyr
NM_001346813.1:c.4805C>A	NP_001333742.1:p.Ser1602Tyr
NM_001363725.1:c.2555C>A	NP_001350654.1:p.Ser852Tyr
XM_011535984.2:c.5015C>A	XP_011534286.2:p.Ser1672Tyr
XM_011535988.3:c.1946C>A	XP_011534290.1:p.Ser649Tyr
XM_017011103.2:c.4916C>A	XP_016866592.1:p.Ser1639Tyr
XM_017011104.1:c.4886C>A	XP_016866593.1:p.Ser1629Tyr
XM_017011105.2:c.4856C>A	XP_016866594.1:p.Ser1619Tyr
XM_017011106.2:c.4727C>A	XP_016866595.1:p.Ser1576Tyr
XM_017011107.2:c.4706C>A	XP_016866596.1:p.Ser1569Tyr
XR_002956289.1:n.5001C>A
NM_001363725.2:c.2555C>A	NP_001350654.1:p.Ser852Tyr
NM_001371656.1:c.4934C>A	NP_001358585.1:p.Ser1645Tyr
NM_001374820.1:c.4934C>A	NP_001361749.1:p.Ser1645Tyr
NM_001374828.1:c.5054C>A MANE Select	NP_001361757.1:p.Ser1685Tyr
NM_017519.3:c.4895C>A	NP_059989.3:p.Ser1632Tyr