Canonical Allele Identifier: CA366227709

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157502202T>G (hg19) ; chr6:g.157181068T>G (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3445T>G	ENSP00000055163.8:p.Phe1149Val
ENST00000414678.8:c.3514T>G	ENSP00000412835.3:p.Phe1172Val
ENST00000637015.2:c.3733T>G	ENSP00000489729.2:p.Phe1245Val
ENST00000319584.11:c.1618T>G	ENSP00000313006.7:p.Phe540Val
ENST00000346085.10:c.3484T>G	ENSP00000344546.5:p.Phe1162Val
ENST00000350026.10:c.3196T>G	ENSP00000055163.7:p.Phe1066Val
ENST00000414678.7:c.1762T>G	ENSP00000412835.2:p.Phe588Val
ENST00000635849.1:c.925T>G	ENSP00000490948.1:p.Phe309Val
ENST00000635957.1:c.559T>G	ENSP00000490385.1:p.Phe187Val
ENST00000636930.2:c.3604T>G MANE Select	ENSP00000490491.2:p.Phe1202Val
ENST00000636940.1:n.1601T>G
ENST00000637015.1:c.972T>G
ENST00000637568.1:c.886T>G
ENST00000637741.1:n.270T>G
ENST00000637810.1:c.946T>G	ENSP00000489636.1:p.Phe316Val
ENST00000637904.1:c.1105T>G	ENSP00000490550.1:p.Phe369Val
ENST00000647938.1:c.3235T>G	ENSP00000498155.1:p.Phe1079Val
ENST00000319584.10:c.1621T>G	ENSP00000313006.6:p.Phe541Val
ENST00000346085.9:c.3235T>G	ENSP00000344546.4:p.Phe1079Val
ENST00000350026.9:c.3196T>G	ENSP00000055163.7:p.Phe1066Val
ENST00000400790.3:c.397T>G	ENSP00000383596.3:p.Phe133Val
ENST00000414678.6:c.1762T>G	ENSP00000412835.2:p.Phe588Val
ENST00000478761.3:c.806T>G
NM_017519.2:c.3196T>G	NP_059989.2:p.Phe1066Val
NM_020732.3:c.3235T>G	NP_065783.3:p.Phe1079Val
XM_005267069.3:c.3355T>G	XP_005267126.2:p.Phe1119Val
XM_011535984.1:c.2434T>G	XP_011534286.1:p.Phe812Val
XM_011535985.1:c.2254T>G	XP_011534287.1:p.Phe752Val
XM_011535986.1:c.2014T>G	XP_011534288.1:p.Phe672Val
XM_011535987.1:c.1633T>G	XP_011534289.1:p.Phe545Val
XM_011535988.1:c.496T>G	XP_011534290.1:p.Phe166Val
NM_001346813.1:c.3355T>G	NP_001333742.1:p.Phe1119Val
NM_001363725.1:c.1105T>G	NP_001350654.1:p.Phe369Val
XM_011535984.2:c.3565T>G	XP_011534286.2:p.Phe1189Val
XM_011535988.3:c.496T>G	XP_011534290.1:p.Phe166Val
XM_017011103.2:c.3466T>G	XP_016866592.1:p.Phe1156Val
XM_017011104.1:c.3436T>G	XP_016866593.1:p.Phe1146Val
XM_017011105.2:c.3406T>G	XP_016866594.1:p.Phe1136Val
XM_017011106.2:c.3277T>G	XP_016866595.1:p.Phe1093Val
XM_017011107.2:c.3256T>G	XP_016866596.1:p.Phe1086Val
XR_002956289.1:n.3648T>G
NM_001363725.2:c.1105T>G	NP_001350654.1:p.Phe369Val
NM_001371656.1:c.3484T>G	NP_001358585.1:p.Phe1162Val
NM_001374820.1:c.3484T>G	NP_001361749.1:p.Phe1162Val
NM_001374828.1:c.3604T>G MANE Select	NP_001361757.1:p.Phe1202Val
NM_017519.3:c.3445T>G	NP_059989.3:p.Phe1149Val