Canonical Allele Identifier: CA366234033

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510795A>T (hg19) ; chr6:g.157189661A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189661A>T , CM000668.2:g.157189661A>T	GRCh38
NC_000006.11:g.157510795A>T , CM000668.1:g.157510795A>T	GRCh37
NC_000006.10:g.157552487A>T	NCBI36
NG_032093.1:g.416732A>T
NG_032093.2:g.416732A>T
NG_066624.1:g.418636A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3780A>T	ENSP00000055163.8:p.Gln1260His
ENST00000414678.8:c.3849A>T	ENSP00000412835.3:p.Gln1283His
ENST00000637015.2:c.4068A>T	ENSP00000489729.2:p.Gln1356His
ENST00000346085.10:c.3819A>T	ENSP00000344546.5:p.Gln1273His
ENST00000350026.10:c.3531A>T	ENSP00000055163.7:p.Gln1177His
ENST00000414678.7:c.2097A>T	ENSP00000412835.2:p.Gln699His
ENST00000635849.1:c.1260A>T	ENSP00000490948.1:p.Gln420His
ENST00000635957.1:c.894A>T	ENSP00000490385.1:p.Gln298His
ENST00000636930.2:c.3939A>T MANE Select	ENSP00000490491.2:p.Gln1313His
ENST00000636940.1:n.1936A>T
ENST00000637015.1:c.1307A>T
ENST00000637568.1:c.1221A>T
ENST00000637741.1:n.605A>T
ENST00000637810.1:c.1281A>T	ENSP00000489636.1:p.Gln427His
ENST00000637904.1:c.1440A>T	ENSP00000490550.1:p.Gln480His
ENST00000647938.1:c.3570A>T	ENSP00000498155.1:p.Gln1190His
ENST00000346085.9:c.3570A>T	ENSP00000344546.4:p.Gln1190His
ENST00000350026.9:c.3531A>T	ENSP00000055163.7:p.Gln1177His
ENST00000414678.6:c.2097A>T	ENSP00000412835.2:p.Gln699His
NM_017519.2:c.3531A>T	NP_059989.2:p.Gln1177His
NM_020732.3:c.3570A>T	NP_065783.3:p.Gln1190His
XM_005267069.3:c.3690A>T	XP_005267126.2:p.Gln1230His
XM_011535984.1:c.2769A>T	XP_011534286.1:p.Gln923His
XM_011535985.1:c.2589A>T	XP_011534287.1:p.Gln863His
XM_011535986.1:c.2349A>T	XP_011534288.1:p.Gln783His
XM_011535987.1:c.1968A>T	XP_011534289.1:p.Gln656His
XM_011535988.1:c.831A>T	XP_011534290.1:p.Gln277His
NM_001346813.1:c.3690A>T	NP_001333742.1:p.Gln1230His
NM_001363725.1:c.1440A>T	NP_001350654.1:p.Gln480His
XM_011535984.2:c.3900A>T	XP_011534286.2:p.Gln1300His
XM_011535988.3:c.831A>T	XP_011534290.1:p.Gln277His
XM_017011103.2:c.3801A>T	XP_016866592.1:p.Gln1267His
XM_017011104.1:c.3771A>T	XP_016866593.1:p.Gln1257His
XM_017011105.2:c.3741A>T	XP_016866594.1:p.Gln1247His
XM_017011106.2:c.3612A>T	XP_016866595.1:p.Gln1204His
XM_017011107.2:c.3591A>T	XP_016866596.1:p.Gln1197His
XR_002956289.1:n.3983A>T
NM_001363725.2:c.1440A>T	NP_001350654.1:p.Gln480His
NM_001371656.1:c.3819A>T	NP_001358585.1:p.Gln1273His
NM_001374820.1:c.3819A>T	NP_001361749.1:p.Gln1273His
NM_001374828.1:c.3939A>T MANE Select	NP_001361757.1:p.Gln1313His
NM_017519.3:c.3780A>T	NP_059989.3:p.Gln1260His