Canonical Allele Identifier: CA452781518

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510822C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189688C>G , CM000668.2:g.157189688C>G	GRCh38
NC_000006.11:g.157510822C>G , CM000668.1:g.157510822C>G	GRCh37
NC_000006.10:g.157552514C>G	NCBI36
NG_032093.1:g.416759C>G
NG_032093.2:g.416759C>G
NG_066624.1:g.418663C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3807C>G	ENSP00000055163.8:p.Gly1269=
ENST00000414678.8:c.3876C>G	ENSP00000412835.3:p.Gly1292=
ENST00000637015.2:c.4095C>G	ENSP00000489729.2:p.Gly1365=
ENST00000346085.10:c.3846C>G	ENSP00000344546.5:p.Gly1282=
ENST00000350026.10:c.3558C>G	ENSP00000055163.7:p.Gly1186=
ENST00000414678.7:c.2124C>G	ENSP00000412835.2:p.Gly708=
ENST00000635849.1:c.1287C>G	ENSP00000490948.1:p.Gly429=
ENST00000635957.1:c.921C>G	ENSP00000490385.1:p.Gly307=
ENST00000636930.2:c.3966C>G MANE Select	ENSP00000490491.2:p.Gly1322=
ENST00000636940.1:n.1963C>G
ENST00000637015.1:c.1334C>G
ENST00000637568.1:c.1248C>G
ENST00000637741.1:n.632C>G
ENST00000637810.1:c.1308C>G	ENSP00000489636.1:p.Gly436=
ENST00000637904.1:c.1467C>G	ENSP00000490550.1:p.Gly489=
ENST00000647938.1:c.3597C>G	ENSP00000498155.1:p.Gly1199=
ENST00000346085.9:c.3597C>G	ENSP00000344546.4:p.Gly1199=
ENST00000350026.9:c.3558C>G	ENSP00000055163.7:p.Gly1186=
ENST00000414678.6:c.2124C>G	ENSP00000412835.2:p.Gly708=
NM_017519.2:c.3558C>G	NP_059989.2:p.Gly1186=
NM_020732.3:c.3597C>G	NP_065783.3:p.Gly1199=
XM_005267069.3:c.3717C>G	XP_005267126.2:p.Gly1239=
XM_011535984.1:c.2796C>G	XP_011534286.1:p.Gly932=
XM_011535985.1:c.2616C>G	XP_011534287.1:p.Gly872=
XM_011535986.1:c.2376C>G	XP_011534288.1:p.Gly792=
XM_011535987.1:c.1995C>G	XP_011534289.1:p.Gly665=
XM_011535988.1:c.858C>G	XP_011534290.1:p.Gly286=
NM_001346813.1:c.3717C>G	NP_001333742.1:p.Gly1239=
NM_001363725.1:c.1467C>G	NP_001350654.1:p.Gly489=
XM_011535984.2:c.3927C>G	XP_011534286.2:p.Gly1309=
XM_011535988.3:c.858C>G	XP_011534290.1:p.Gly286=
XM_017011103.2:c.3828C>G	XP_016866592.1:p.Gly1276=
XM_017011104.1:c.3798C>G	XP_016866593.1:p.Gly1266=
XM_017011105.2:c.3768C>G	XP_016866594.1:p.Gly1256=
XM_017011106.2:c.3639C>G	XP_016866595.1:p.Gly1213=
XM_017011107.2:c.3618C>G	XP_016866596.1:p.Gly1206=
XR_002956289.1:n.4010C>G
NM_001363725.2:c.1467C>G	NP_001350654.1:p.Gly489=
NM_001371656.1:c.3846C>G	NP_001358585.1:p.Gly1282=
NM_001374820.1:c.3846C>G	NP_001361749.1:p.Gly1282=
NM_001374828.1:c.3966C>G MANE Select	NP_001361757.1:p.Gly1322=
NM_017519.3:c.3807C>G	NP_059989.3:p.Gly1269=