Canonical Allele Identifier: CA366242394

Gene: ARID1B

Linked Data

• dbSNP Id: rs1277541274
• MyVariant Identifiers: chr6:g.157522413C>G (hg19) ; chr6:g.157201279C>G (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4895C>G	ENSP00000055163.8:p.Ser1632Cys
ENST00000414678.8:c.4964C>G	ENSP00000412835.3:p.Ser1655Cys
ENST00000637015.2:c.5183C>G	ENSP00000489729.2:p.Ser1728Cys
ENST00000346085.10:c.4934C>G	ENSP00000344546.5:p.Ser1645Cys
ENST00000350026.10:c.4646C>G	ENSP00000055163.7:p.Ser1549Cys
ENST00000414678.7:c.3212C>G	ENSP00000412835.2:p.Ser1071Cys
ENST00000635849.1:c.2375C>G	ENSP00000490948.1:p.Ser792Cys
ENST00000635957.1:c.2006C>G	ENSP00000490385.1:p.Ser669Cys
ENST00000636227.1:n.3517C>G
ENST00000636254.1:n.974C>G
ENST00000636930.2:c.5054C>G MANE Select	ENSP00000490491.2:p.Ser1685Cys
ENST00000636940.1:n.3051C>G
ENST00000637015.1:c.2422C>G
ENST00000637568.1:c.2336C>G
ENST00000637741.1:n.1720C>G
ENST00000637810.1:c.2396C>G	ENSP00000489636.1:p.Ser799Cys
ENST00000637904.1:c.2555C>G	ENSP00000490550.1:p.Ser852Cys
ENST00000647938.1:c.4685C>G	ENSP00000498155.1:p.Ser1562Cys
ENST00000346085.9:c.4685C>G	ENSP00000344546.4:p.Ser1562Cys
ENST00000350026.9:c.4646C>G	ENSP00000055163.7:p.Ser1549Cys
ENST00000414678.6:c.3212C>G	ENSP00000412835.2:p.Ser1071Cys
NM_017519.2:c.4646C>G	NP_059989.2:p.Ser1549Cys
NM_020732.3:c.4685C>G	NP_065783.3:p.Ser1562Cys
XM_005267069.3:c.4805C>G	XP_005267126.2:p.Ser1602Cys
XM_011535984.1:c.3884C>G	XP_011534286.1:p.Ser1295Cys
XM_011535985.1:c.3704C>G	XP_011534287.1:p.Ser1235Cys
XM_011535986.1:c.3464C>G	XP_011534288.1:p.Ser1155Cys
XM_011535987.1:c.3083C>G	XP_011534289.1:p.Ser1028Cys
XM_011535988.1:c.1946C>G	XP_011534290.1:p.Ser649Cys
NM_001346813.1:c.4805C>G	NP_001333742.1:p.Ser1602Cys
NM_001363725.1:c.2555C>G	NP_001350654.1:p.Ser852Cys
XM_011535984.2:c.5015C>G	XP_011534286.2:p.Ser1672Cys
XM_011535988.3:c.1946C>G	XP_011534290.1:p.Ser649Cys
XM_017011103.2:c.4916C>G	XP_016866592.1:p.Ser1639Cys
XM_017011104.1:c.4886C>G	XP_016866593.1:p.Ser1629Cys
XM_017011105.2:c.4856C>G	XP_016866594.1:p.Ser1619Cys
XM_017011106.2:c.4727C>G	XP_016866595.1:p.Ser1576Cys
XM_017011107.2:c.4706C>G	XP_016866596.1:p.Ser1569Cys
XR_002956289.1:n.5001C>G
NM_001363725.2:c.2555C>G	NP_001350654.1:p.Ser852Cys
NM_001371656.1:c.4934C>G	NP_001358585.1:p.Ser1645Cys
NM_001374820.1:c.4934C>G	NP_001361749.1:p.Ser1645Cys
NM_001374828.1:c.5054C>G MANE Select	NP_001361757.1:p.Ser1685Cys
NM_017519.3:c.4895C>G	NP_059989.3:p.Ser1632Cys