Canonical Allele Identifier: CA366227705

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128317190
• MyVariant Identifiers: chr6:g.157502202T>A (hg19) ; chr6:g.157181068T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181068T>A , CM000668.2:g.157181068T>A	GRCh38
NC_000006.11:g.157502202T>A , CM000668.1:g.157502202T>A	GRCh37
NC_000006.10:g.157543894T>A	NCBI36
NG_032093.1:g.408139T>A
NG_032093.2:g.408139T>A
NG_066624.1:g.410043T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3445T>A	ENSP00000055163.8:p.Phe1149Ile
ENST00000414678.8:c.3514T>A	ENSP00000412835.3:p.Phe1172Ile
ENST00000637015.2:c.3733T>A	ENSP00000489729.2:p.Phe1245Ile
ENST00000319584.11:c.1618T>A	ENSP00000313006.7:p.Phe540Ile
ENST00000346085.10:c.3484T>A	ENSP00000344546.5:p.Phe1162Ile
ENST00000350026.10:c.3196T>A	ENSP00000055163.7:p.Phe1066Ile
ENST00000414678.7:c.1762T>A	ENSP00000412835.2:p.Phe588Ile
ENST00000635849.1:c.925T>A	ENSP00000490948.1:p.Phe309Ile
ENST00000635957.1:c.559T>A	ENSP00000490385.1:p.Phe187Ile
ENST00000636930.2:c.3604T>A MANE Select	ENSP00000490491.2:p.Phe1202Ile
ENST00000636940.1:n.1601T>A
ENST00000637015.1:c.972T>A
ENST00000637568.1:c.886T>A
ENST00000637741.1:n.270T>A
ENST00000637810.1:c.946T>A	ENSP00000489636.1:p.Phe316Ile
ENST00000637904.1:c.1105T>A	ENSP00000490550.1:p.Phe369Ile
ENST00000647938.1:c.3235T>A	ENSP00000498155.1:p.Phe1079Ile
ENST00000319584.10:c.1621T>A	ENSP00000313006.6:p.Phe541Ile
ENST00000346085.9:c.3235T>A	ENSP00000344546.4:p.Phe1079Ile
ENST00000350026.9:c.3196T>A	ENSP00000055163.7:p.Phe1066Ile
ENST00000400790.3:c.397T>A	ENSP00000383596.3:p.Phe133Ile
ENST00000414678.6:c.1762T>A	ENSP00000412835.2:p.Phe588Ile
ENST00000478761.3:c.806T>A
NM_017519.2:c.3196T>A	NP_059989.2:p.Phe1066Ile
NM_020732.3:c.3235T>A	NP_065783.3:p.Phe1079Ile
XM_005267069.3:c.3355T>A	XP_005267126.2:p.Phe1119Ile
XM_011535984.1:c.2434T>A	XP_011534286.1:p.Phe812Ile
XM_011535985.1:c.2254T>A	XP_011534287.1:p.Phe752Ile
XM_011535986.1:c.2014T>A	XP_011534288.1:p.Phe672Ile
XM_011535987.1:c.1633T>A	XP_011534289.1:p.Phe545Ile
XM_011535988.1:c.496T>A	XP_011534290.1:p.Phe166Ile
NM_001346813.1:c.3355T>A	NP_001333742.1:p.Phe1119Ile
NM_001363725.1:c.1105T>A	NP_001350654.1:p.Phe369Ile
XM_011535984.2:c.3565T>A	XP_011534286.2:p.Phe1189Ile
XM_011535988.3:c.496T>A	XP_011534290.1:p.Phe166Ile
XM_017011103.2:c.3466T>A	XP_016866592.1:p.Phe1156Ile
XM_017011104.1:c.3436T>A	XP_016866593.1:p.Phe1146Ile
XM_017011105.2:c.3406T>A	XP_016866594.1:p.Phe1136Ile
XM_017011106.2:c.3277T>A	XP_016866595.1:p.Phe1093Ile
XM_017011107.2:c.3256T>A	XP_016866596.1:p.Phe1086Ile
XR_002956289.1:n.3648T>A
NM_001363725.2:c.1105T>A	NP_001350654.1:p.Phe369Ile
NM_001371656.1:c.3484T>A	NP_001358585.1:p.Phe1162Ile
NM_001374820.1:c.3484T>A	NP_001361749.1:p.Phe1162Ile
NM_001374828.1:c.3604T>A MANE Select	NP_001361757.1:p.Phe1202Ile
NM_017519.3:c.3445T>A	NP_059989.3:p.Phe1149Ile