Canonical Allele Identifier: CA366242814

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522509G>T (hg19) ; chr6:g.157201375G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201375G>T , CM000668.2:g.157201375G>T	GRCh38
NC_000006.11:g.157522509G>T , CM000668.1:g.157522509G>T	GRCh37
NC_000006.10:g.157564201G>T	NCBI36
NG_032093.1:g.428446G>T
NG_032093.2:g.428446G>T
NG_066624.1:g.430350G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4991G>T	ENSP00000055163.8:p.Gly1664Val
ENST00000414678.8:c.5060G>T	ENSP00000412835.3:p.Gly1687Val
ENST00000637015.2:c.5279G>T	ENSP00000489729.2:p.Gly1760Val
ENST00000346085.10:c.5030G>T	ENSP00000344546.5:p.Gly1677Val
ENST00000350026.10:c.4742G>T	ENSP00000055163.7:p.Gly1581Val
ENST00000414678.7:c.3308G>T	ENSP00000412835.2:p.Gly1103Val
ENST00000635849.1:c.2471G>T	ENSP00000490948.1:p.Gly824Val
ENST00000635957.1:c.2102G>T	ENSP00000490385.1:p.Gly701Val
ENST00000636227.1:n.3613G>T
ENST00000636254.1:n.1070G>T
ENST00000636930.2:c.5150G>T MANE Select	ENSP00000490491.2:p.Gly1717Val
ENST00000636940.1:n.3147G>T
ENST00000637015.1:c.2518G>T
ENST00000637568.1:c.2432G>T
ENST00000637741.1:n.1816G>T
ENST00000637810.1:c.2492G>T	ENSP00000489636.1:p.Gly831Val
ENST00000637904.1:c.2651G>T	ENSP00000490550.1:p.Gly884Val
ENST00000647938.1:c.4781G>T	ENSP00000498155.1:p.Gly1594Val
ENST00000346085.9:c.4781G>T	ENSP00000344546.4:p.Gly1594Val
ENST00000350026.9:c.4742G>T	ENSP00000055163.7:p.Gly1581Val
ENST00000414678.6:c.3308G>T	ENSP00000412835.2:p.Gly1103Val
NM_017519.2:c.4742G>T	NP_059989.2:p.Gly1581Val
NM_020732.3:c.4781G>T	NP_065783.3:p.Gly1594Val
XM_005267069.3:c.4901G>T	XP_005267126.2:p.Gly1634Val
XM_011535984.1:c.3980G>T	XP_011534286.1:p.Gly1327Val
XM_011535985.1:c.3800G>T	XP_011534287.1:p.Gly1267Val
XM_011535986.1:c.3560G>T	XP_011534288.1:p.Gly1187Val
XM_011535987.1:c.3179G>T	XP_011534289.1:p.Gly1060Val
XM_011535988.1:c.2042G>T	XP_011534290.1:p.Gly681Val
NM_001346813.1:c.4901G>T	NP_001333742.1:p.Gly1634Val
NM_001363725.1:c.2651G>T	NP_001350654.1:p.Gly884Val
XM_011535984.2:c.5111G>T	XP_011534286.2:p.Gly1704Val
XM_011535988.3:c.2042G>T	XP_011534290.1:p.Gly681Val
XM_017011103.2:c.5012G>T	XP_016866592.1:p.Gly1671Val
XM_017011104.1:c.4982G>T	XP_016866593.1:p.Gly1661Val
XM_017011105.2:c.4952G>T	XP_016866594.1:p.Gly1651Val
XM_017011106.2:c.4823G>T	XP_016866595.1:p.Gly1608Val
XM_017011107.2:c.4802G>T	XP_016866596.1:p.Gly1601Val
XR_002956289.1:n.5097G>T
NM_001363725.2:c.2651G>T	NP_001350654.1:p.Gly884Val
NM_001371656.1:c.5030G>T	NP_001358585.1:p.Gly1677Val
NM_001374820.1:c.5030G>T	NP_001361749.1:p.Gly1677Val
NM_001374828.1:c.5150G>T MANE Select	NP_001361757.1:p.Gly1717Val
NM_017519.3:c.4991G>T	NP_059989.3:p.Gly1664Val