Canonical Allele Identifier: CA366234670

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157511180C>G (hg19) ; chr6:g.157190046C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190046C>G , CM000668.2:g.157190046C>G	GRCh38
NC_000006.11:g.157511180C>G , CM000668.1:g.157511180C>G	GRCh37
NC_000006.10:g.157552872C>G	NCBI36
NG_032093.1:g.417117C>G
NG_032093.2:g.417117C>G
NG_066624.1:g.419021C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3908C>G	ENSP00000055163.8:p.Thr1303Arg
ENST00000414678.8:c.3977C>G	ENSP00000412835.3:p.Thr1326Arg
ENST00000637015.2:c.4196C>G	ENSP00000489729.2:p.Thr1399Arg
ENST00000346085.10:c.3947C>G	ENSP00000344546.5:p.Thr1316Arg
ENST00000350026.10:c.3659C>G	ENSP00000055163.7:p.Thr1220Arg
ENST00000414678.7:c.2225C>G	ENSP00000412835.2:p.Thr742Arg
ENST00000635849.1:c.1388C>G	ENSP00000490948.1:p.Thr463Arg
ENST00000635957.1:c.1019C>G	ENSP00000490385.1:p.Thr340Arg
ENST00000636930.2:c.4067C>G MANE Select	ENSP00000490491.2:p.Thr1356Arg
ENST00000636940.1:n.2064C>G
ENST00000637015.1:c.1435C>G
ENST00000637568.1:c.1349C>G
ENST00000637741.1:n.733C>G
ENST00000637810.1:c.1409C>G	ENSP00000489636.1:p.Thr470Arg
ENST00000637904.1:c.1568C>G	ENSP00000490550.1:p.Thr523Arg
ENST00000647938.1:c.3698C>G	ENSP00000498155.1:p.Thr1233Arg
ENST00000346085.9:c.3698C>G	ENSP00000344546.4:p.Thr1233Arg
ENST00000350026.9:c.3659C>G	ENSP00000055163.7:p.Thr1220Arg
ENST00000414678.6:c.2225C>G	ENSP00000412835.2:p.Thr742Arg
NM_017519.2:c.3659C>G	NP_059989.2:p.Thr1220Arg
NM_020732.3:c.3698C>G	NP_065783.3:p.Thr1233Arg
XM_005267069.3:c.3818C>G	XP_005267126.2:p.Thr1273Arg
XM_011535984.1:c.2897C>G	XP_011534286.1:p.Thr966Arg
XM_011535985.1:c.2717C>G	XP_011534287.1:p.Thr906Arg
XM_011535986.1:c.2477C>G	XP_011534288.1:p.Thr826Arg
XM_011535987.1:c.2096C>G	XP_011534289.1:p.Thr699Arg
XM_011535988.1:c.959C>G	XP_011534290.1:p.Thr320Arg
NM_001346813.1:c.3818C>G	NP_001333742.1:p.Thr1273Arg
NM_001363725.1:c.1568C>G	NP_001350654.1:p.Thr523Arg
XM_011535984.2:c.4028C>G	XP_011534286.2:p.Thr1343Arg
XM_011535988.3:c.959C>G	XP_011534290.1:p.Thr320Arg
XM_017011103.2:c.3929C>G	XP_016866592.1:p.Thr1310Arg
XM_017011104.1:c.3899C>G	XP_016866593.1:p.Thr1300Arg
XM_017011105.2:c.3869C>G	XP_016866594.1:p.Thr1290Arg
XM_017011106.2:c.3740C>G	XP_016866595.1:p.Thr1247Arg
XM_017011107.2:c.3719C>G	XP_016866596.1:p.Thr1240Arg
XR_002956289.1:n.4111C>G
NM_001363725.2:c.1568C>G	NP_001350654.1:p.Thr523Arg
NM_001371656.1:c.3947C>G	NP_001358585.1:p.Thr1316Arg
NM_001374820.1:c.3947C>G	NP_001361749.1:p.Thr1316Arg
NM_001374828.1:c.4067C>G MANE Select	NP_001361757.1:p.Thr1356Arg
NM_017519.3:c.3908C>G	NP_059989.3:p.Thr1303Arg