Canonical Allele Identifier: CA366228234

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128317612
• MyVariant Identifiers: chr6:g.157502268T>A (hg19) ; chr6:g.157181134T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181134T>A , CM000668.2:g.157181134T>A	GRCh38
NC_000006.11:g.157502268T>A , CM000668.1:g.157502268T>A	GRCh37
NC_000006.10:g.157543960T>A	NCBI36
NG_032093.1:g.408205T>A
NG_032093.2:g.408205T>A
NG_066624.1:g.410109T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3511T>A	ENSP00000055163.8:p.Phe1171Ile
ENST00000414678.8:c.3580T>A	ENSP00000412835.3:p.Phe1194Ile
ENST00000637015.2:c.3799T>A	ENSP00000489729.2:p.Phe1267Ile
ENST00000319584.11:c.1684T>A	ENSP00000313006.7:p.Phe562Ile
ENST00000346085.10:c.3550T>A	ENSP00000344546.5:p.Phe1184Ile
ENST00000350026.10:c.3262T>A	ENSP00000055163.7:p.Phe1088Ile
ENST00000414678.7:c.1828T>A	ENSP00000412835.2:p.Phe610Ile
ENST00000635849.1:c.991T>A	ENSP00000490948.1:p.Phe331Ile
ENST00000635957.1:c.625T>A	ENSP00000490385.1:p.Phe209Ile
ENST00000636930.2:c.3670T>A MANE Select	ENSP00000490491.2:p.Phe1224Ile
ENST00000636940.1:n.1667T>A
ENST00000637015.1:c.1038T>A
ENST00000637568.1:c.952T>A
ENST00000637741.1:n.336T>A
ENST00000637810.1:c.1012T>A	ENSP00000489636.1:p.Phe338Ile
ENST00000637904.1:c.1171T>A	ENSP00000490550.1:p.Phe391Ile
ENST00000647938.1:c.3301T>A	ENSP00000498155.1:p.Phe1101Ile
ENST00000319584.10:c.1687T>A	ENSP00000313006.6:p.Phe563Ile
ENST00000346085.9:c.3301T>A	ENSP00000344546.4:p.Phe1101Ile
ENST00000350026.9:c.3262T>A	ENSP00000055163.7:p.Phe1088Ile
ENST00000400790.3:c.463T>A	ENSP00000383596.3:p.Phe155Ile
ENST00000414678.6:c.1828T>A	ENSP00000412835.2:p.Phe610Ile
ENST00000478761.3:c.872T>A
NM_017519.2:c.3262T>A	NP_059989.2:p.Phe1088Ile
NM_020732.3:c.3301T>A	NP_065783.3:p.Phe1101Ile
XM_005267069.3:c.3421T>A	XP_005267126.2:p.Phe1141Ile
XM_011535984.1:c.2500T>A	XP_011534286.1:p.Phe834Ile
XM_011535985.1:c.2320T>A	XP_011534287.1:p.Phe774Ile
XM_011535986.1:c.2080T>A	XP_011534288.1:p.Phe694Ile
XM_011535987.1:c.1699T>A	XP_011534289.1:p.Phe567Ile
XM_011535988.1:c.562T>A	XP_011534290.1:p.Phe188Ile
NM_001346813.1:c.3421T>A	NP_001333742.1:p.Phe1141Ile
NM_001363725.1:c.1171T>A	NP_001350654.1:p.Phe391Ile
XM_011535984.2:c.3631T>A	XP_011534286.2:p.Phe1211Ile
XM_011535988.3:c.562T>A	XP_011534290.1:p.Phe188Ile
XM_017011103.2:c.3532T>A	XP_016866592.1:p.Phe1178Ile
XM_017011104.1:c.3502T>A	XP_016866593.1:p.Phe1168Ile
XM_017011105.2:c.3472T>A	XP_016866594.1:p.Phe1158Ile
XM_017011106.2:c.3343T>A	XP_016866595.1:p.Phe1115Ile
XM_017011107.2:c.3322T>A	XP_016866596.1:p.Phe1108Ile
XR_002956289.1:n.3714T>A
NM_001363725.2:c.1171T>A	NP_001350654.1:p.Phe391Ile
NM_001371656.1:c.3550T>A	NP_001358585.1:p.Phe1184Ile
NM_001374820.1:c.3550T>A	NP_001361749.1:p.Phe1184Ile
NM_001374828.1:c.3670T>A MANE Select	NP_001361757.1:p.Phe1224Ile
NM_017519.3:c.3511T>A	NP_059989.3:p.Phe1171Ile