Canonical Allele Identifier: CA366242373

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522404T>G (hg19) ; chr6:g.157201270T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201270T>G , CM000668.2:g.157201270T>G	GRCh38
NC_000006.11:g.157522404T>G , CM000668.1:g.157522404T>G	GRCh37
NC_000006.10:g.157564096T>G	NCBI36
NG_032093.1:g.428341T>G
NG_032093.2:g.428341T>G
NG_066624.1:g.430245T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4886T>G	ENSP00000055163.8:p.Phe1629Cys
ENST00000414678.8:c.4955T>G	ENSP00000412835.3:p.Phe1652Cys
ENST00000637015.2:c.5174T>G	ENSP00000489729.2:p.Phe1725Cys
ENST00000346085.10:c.4925T>G	ENSP00000344546.5:p.Phe1642Cys
ENST00000350026.10:c.4637T>G	ENSP00000055163.7:p.Phe1546Cys
ENST00000414678.7:c.3203T>G	ENSP00000412835.2:p.Phe1068Cys
ENST00000635849.1:c.2366T>G	ENSP00000490948.1:p.Phe789Cys
ENST00000635957.1:c.1997T>G	ENSP00000490385.1:p.Phe666Cys
ENST00000636227.1:n.3508T>G
ENST00000636254.1:n.965T>G
ENST00000636930.2:c.5045T>G MANE Select	ENSP00000490491.2:p.Phe1682Cys
ENST00000636940.1:n.3042T>G
ENST00000637015.1:c.2413T>G
ENST00000637568.1:c.2327T>G
ENST00000637741.1:n.1711T>G
ENST00000637810.1:c.2387T>G	ENSP00000489636.1:p.Phe796Cys
ENST00000637904.1:c.2546T>G	ENSP00000490550.1:p.Phe849Cys
ENST00000647938.1:c.4676T>G	ENSP00000498155.1:p.Phe1559Cys
ENST00000346085.9:c.4676T>G	ENSP00000344546.4:p.Phe1559Cys
ENST00000350026.9:c.4637T>G	ENSP00000055163.7:p.Phe1546Cys
ENST00000414678.6:c.3203T>G	ENSP00000412835.2:p.Phe1068Cys
NM_017519.2:c.4637T>G	NP_059989.2:p.Phe1546Cys
NM_020732.3:c.4676T>G	NP_065783.3:p.Phe1559Cys
XM_005267069.3:c.4796T>G	XP_005267126.2:p.Phe1599Cys
XM_011535984.1:c.3875T>G	XP_011534286.1:p.Phe1292Cys
XM_011535985.1:c.3695T>G	XP_011534287.1:p.Phe1232Cys
XM_011535986.1:c.3455T>G	XP_011534288.1:p.Phe1152Cys
XM_011535987.1:c.3074T>G	XP_011534289.1:p.Phe1025Cys
XM_011535988.1:c.1937T>G	XP_011534290.1:p.Phe646Cys
NM_001346813.1:c.4796T>G	NP_001333742.1:p.Phe1599Cys
NM_001363725.1:c.2546T>G	NP_001350654.1:p.Phe849Cys
XM_011535984.2:c.5006T>G	XP_011534286.2:p.Phe1669Cys
XM_011535988.3:c.1937T>G	XP_011534290.1:p.Phe646Cys
XM_017011103.2:c.4907T>G	XP_016866592.1:p.Phe1636Cys
XM_017011104.1:c.4877T>G	XP_016866593.1:p.Phe1626Cys
XM_017011105.2:c.4847T>G	XP_016866594.1:p.Phe1616Cys
XM_017011106.2:c.4718T>G	XP_016866595.1:p.Phe1573Cys
XM_017011107.2:c.4697T>G	XP_016866596.1:p.Phe1566Cys
XR_002956289.1:n.4992T>G
NM_001363725.2:c.2546T>G	NP_001350654.1:p.Phe849Cys
NM_001371656.1:c.4925T>G	NP_001358585.1:p.Phe1642Cys
NM_001374820.1:c.4925T>G	NP_001361749.1:p.Phe1642Cys
NM_001374828.1:c.5045T>G MANE Select	NP_001361757.1:p.Phe1682Cys
NM_017519.3:c.4886T>G	NP_059989.3:p.Phe1629Cys