Canonical Allele Identifier: CA366228241

Gene: ARID1B

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3511T>G	ENSP00000055163.8:p.Phe1171Val
ENST00000414678.8:c.3580T>G	ENSP00000412835.3:p.Phe1194Val
ENST00000637015.2:c.3799T>G	ENSP00000489729.2:p.Phe1267Val
ENST00000319584.11:c.1684T>G	ENSP00000313006.7:p.Phe562Val
ENST00000346085.10:c.3550T>G	ENSP00000344546.5:p.Phe1184Val
ENST00000350026.10:c.3262T>G	ENSP00000055163.7:p.Phe1088Val
ENST00000414678.7:c.1828T>G	ENSP00000412835.2:p.Phe610Val
ENST00000635849.1:c.991T>G	ENSP00000490948.1:p.Phe331Val
ENST00000635957.1:c.625T>G	ENSP00000490385.1:p.Phe209Val
ENST00000636930.2:c.3670T>G MANE Select	ENSP00000490491.2:p.Phe1224Val
ENST00000636940.1:n.1667T>G
ENST00000637015.1:c.1038T>G
ENST00000637568.1:c.952T>G
ENST00000637741.1:n.336T>G
ENST00000637810.1:c.1012T>G	ENSP00000489636.1:p.Phe338Val
ENST00000637904.1:c.1171T>G	ENSP00000490550.1:p.Phe391Val
ENST00000647938.1:c.3301T>G	ENSP00000498155.1:p.Phe1101Val
ENST00000319584.10:c.1687T>G	ENSP00000313006.6:p.Phe563Val
ENST00000346085.9:c.3301T>G	ENSP00000344546.4:p.Phe1101Val
ENST00000350026.9:c.3262T>G	ENSP00000055163.7:p.Phe1088Val
ENST00000400790.3:c.463T>G	ENSP00000383596.3:p.Phe155Val
ENST00000414678.6:c.1828T>G	ENSP00000412835.2:p.Phe610Val
ENST00000478761.3:c.872T>G
NM_017519.2:c.3262T>G	NP_059989.2:p.Phe1088Val
NM_020732.3:c.3301T>G	NP_065783.3:p.Phe1101Val
XM_005267069.3:c.3421T>G	XP_005267126.2:p.Phe1141Val
XM_011535984.1:c.2500T>G	XP_011534286.1:p.Phe834Val
XM_011535985.1:c.2320T>G	XP_011534287.1:p.Phe774Val
XM_011535986.1:c.2080T>G	XP_011534288.1:p.Phe694Val
XM_011535987.1:c.1699T>G	XP_011534289.1:p.Phe567Val
XM_011535988.1:c.562T>G	XP_011534290.1:p.Phe188Val
NM_001346813.1:c.3421T>G	NP_001333742.1:p.Phe1141Val
NM_001363725.1:c.1171T>G	NP_001350654.1:p.Phe391Val
XM_011535984.2:c.3631T>G	XP_011534286.2:p.Phe1211Val
XM_011535988.3:c.562T>G	XP_011534290.1:p.Phe188Val
XM_017011103.2:c.3532T>G	XP_016866592.1:p.Phe1178Val
XM_017011104.1:c.3502T>G	XP_016866593.1:p.Phe1168Val
XM_017011105.2:c.3472T>G	XP_016866594.1:p.Phe1158Val
XM_017011106.2:c.3343T>G	XP_016866595.1:p.Phe1115Val
XM_017011107.2:c.3322T>G	XP_016866596.1:p.Phe1108Val
XR_002956289.1:n.3714T>G
NM_001363725.2:c.1171T>G	NP_001350654.1:p.Phe391Val
NM_001371656.1:c.3550T>G	NP_001358585.1:p.Phe1184Val
NM_001374820.1:c.3550T>G	NP_001361749.1:p.Phe1184Val
NM_001374828.1:c.3670T>G MANE Select	NP_001361757.1:p.Phe1224Val
NM_017519.3:c.3511T>G	NP_059989.3:p.Phe1171Val