Canonical Allele Identifier: CA366234062

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510809C>G (hg19) ; chr6:g.157189675C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189675C>G , CM000668.2:g.157189675C>G	GRCh38
NC_000006.11:g.157510809C>G , CM000668.1:g.157510809C>G	GRCh37
NC_000006.10:g.157552501C>G	NCBI36
NG_032093.1:g.416746C>G
NG_032093.2:g.416746C>G
NG_066624.1:g.418650C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3794C>G	ENSP00000055163.8:p.Pro1265Arg
ENST00000414678.8:c.3863C>G	ENSP00000412835.3:p.Pro1288Arg
ENST00000637015.2:c.4082C>G	ENSP00000489729.2:p.Pro1361Arg
ENST00000346085.10:c.3833C>G	ENSP00000344546.5:p.Pro1278Arg
ENST00000350026.10:c.3545C>G	ENSP00000055163.7:p.Pro1182Arg
ENST00000414678.7:c.2111C>G	ENSP00000412835.2:p.Pro704Arg
ENST00000635849.1:c.1274C>G	ENSP00000490948.1:p.Pro425Arg
ENST00000635957.1:c.908C>G	ENSP00000490385.1:p.Pro303Arg
ENST00000636930.2:c.3953C>G MANE Select	ENSP00000490491.2:p.Pro1318Arg
ENST00000636940.1:n.1950C>G
ENST00000637015.1:c.1321C>G
ENST00000637568.1:c.1235C>G
ENST00000637741.1:n.619C>G
ENST00000637810.1:c.1295C>G	ENSP00000489636.1:p.Pro432Arg
ENST00000637904.1:c.1454C>G	ENSP00000490550.1:p.Pro485Arg
ENST00000647938.1:c.3584C>G	ENSP00000498155.1:p.Pro1195Arg
ENST00000346085.9:c.3584C>G	ENSP00000344546.4:p.Pro1195Arg
ENST00000350026.9:c.3545C>G	ENSP00000055163.7:p.Pro1182Arg
ENST00000414678.6:c.2111C>G	ENSP00000412835.2:p.Pro704Arg
NM_017519.2:c.3545C>G	NP_059989.2:p.Pro1182Arg
NM_020732.3:c.3584C>G	NP_065783.3:p.Pro1195Arg
XM_005267069.3:c.3704C>G	XP_005267126.2:p.Pro1235Arg
XM_011535984.1:c.2783C>G	XP_011534286.1:p.Pro928Arg
XM_011535985.1:c.2603C>G	XP_011534287.1:p.Pro868Arg
XM_011535986.1:c.2363C>G	XP_011534288.1:p.Pro788Arg
XM_011535987.1:c.1982C>G	XP_011534289.1:p.Pro661Arg
XM_011535988.1:c.845C>G	XP_011534290.1:p.Pro282Arg
NM_001346813.1:c.3704C>G	NP_001333742.1:p.Pro1235Arg
NM_001363725.1:c.1454C>G	NP_001350654.1:p.Pro485Arg
XM_011535984.2:c.3914C>G	XP_011534286.2:p.Pro1305Arg
XM_011535988.3:c.845C>G	XP_011534290.1:p.Pro282Arg
XM_017011103.2:c.3815C>G	XP_016866592.1:p.Pro1272Arg
XM_017011104.1:c.3785C>G	XP_016866593.1:p.Pro1262Arg
XM_017011105.2:c.3755C>G	XP_016866594.1:p.Pro1252Arg
XM_017011106.2:c.3626C>G	XP_016866595.1:p.Pro1209Arg
XM_017011107.2:c.3605C>G	XP_016866596.1:p.Pro1202Arg
XR_002956289.1:n.3997C>G
NM_001363725.2:c.1454C>G	NP_001350654.1:p.Pro485Arg
NM_001371656.1:c.3833C>G	NP_001358585.1:p.Pro1278Arg
NM_001374820.1:c.3833C>G	NP_001361749.1:p.Pro1278Arg
NM_001374828.1:c.3953C>G MANE Select	NP_001361757.1:p.Pro1318Arg
NM_017519.3:c.3794C>G	NP_059989.3:p.Pro1265Arg