Canonical Allele Identifier: CA366242791

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522505A>G (hg19) ; chr6:g.157201371A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201371A>G , CM000668.2:g.157201371A>G	GRCh38
NC_000006.11:g.157522505A>G , CM000668.1:g.157522505A>G	GRCh37
NC_000006.10:g.157564197A>G	NCBI36
NG_032093.1:g.428442A>G
NG_032093.2:g.428442A>G
NG_066624.1:g.430346A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4987A>G	ENSP00000055163.8:p.Thr1663Ala
ENST00000414678.8:c.5056A>G	ENSP00000412835.3:p.Thr1686Ala
ENST00000637015.2:c.5275A>G	ENSP00000489729.2:p.Thr1759Ala
ENST00000346085.10:c.5026A>G	ENSP00000344546.5:p.Thr1676Ala
ENST00000350026.10:c.4738A>G	ENSP00000055163.7:p.Thr1580Ala
ENST00000414678.7:c.3304A>G	ENSP00000412835.2:p.Thr1102Ala
ENST00000635849.1:c.2467A>G	ENSP00000490948.1:p.Thr823Ala
ENST00000635957.1:c.2098A>G	ENSP00000490385.1:p.Thr700Ala
ENST00000636227.1:n.3609A>G
ENST00000636254.1:n.1066A>G
ENST00000636930.2:c.5146A>G MANE Select	ENSP00000490491.2:p.Thr1716Ala
ENST00000636940.1:n.3143A>G
ENST00000637015.1:c.2514A>G
ENST00000637568.1:c.2428A>G
ENST00000637741.1:n.1812A>G
ENST00000637810.1:c.2488A>G	ENSP00000489636.1:p.Thr830Ala
ENST00000637904.1:c.2647A>G	ENSP00000490550.1:p.Thr883Ala
ENST00000647938.1:c.4777A>G	ENSP00000498155.1:p.Thr1593Ala
ENST00000346085.9:c.4777A>G	ENSP00000344546.4:p.Thr1593Ala
ENST00000350026.9:c.4738A>G	ENSP00000055163.7:p.Thr1580Ala
ENST00000414678.6:c.3304A>G	ENSP00000412835.2:p.Thr1102Ala
NM_017519.2:c.4738A>G	NP_059989.2:p.Thr1580Ala
NM_020732.3:c.4777A>G	NP_065783.3:p.Thr1593Ala
XM_005267069.3:c.4897A>G	XP_005267126.2:p.Thr1633Ala
XM_011535984.1:c.3976A>G	XP_011534286.1:p.Thr1326Ala
XM_011535985.1:c.3796A>G	XP_011534287.1:p.Thr1266Ala
XM_011535986.1:c.3556A>G	XP_011534288.1:p.Thr1186Ala
XM_011535987.1:c.3175A>G	XP_011534289.1:p.Thr1059Ala
XM_011535988.1:c.2038A>G	XP_011534290.1:p.Thr680Ala
NM_001346813.1:c.4897A>G	NP_001333742.1:p.Thr1633Ala
NM_001363725.1:c.2647A>G	NP_001350654.1:p.Thr883Ala
XM_011535984.2:c.5107A>G	XP_011534286.2:p.Thr1703Ala
XM_011535988.3:c.2038A>G	XP_011534290.1:p.Thr680Ala
XM_017011103.2:c.5008A>G	XP_016866592.1:p.Thr1670Ala
XM_017011104.1:c.4978A>G	XP_016866593.1:p.Thr1660Ala
XM_017011105.2:c.4948A>G	XP_016866594.1:p.Thr1650Ala
XM_017011106.2:c.4819A>G	XP_016866595.1:p.Thr1607Ala
XM_017011107.2:c.4798A>G	XP_016866596.1:p.Thr1600Ala
XR_002956289.1:n.5093A>G
NM_001363725.2:c.2647A>G	NP_001350654.1:p.Thr883Ala
NM_001371656.1:c.5026A>G	NP_001358585.1:p.Thr1676Ala
NM_001374820.1:c.5026A>G	NP_001361749.1:p.Thr1676Ala
NM_001374828.1:c.5146A>G MANE Select	NP_001361757.1:p.Thr1716Ala
NM_017519.3:c.4987A>G	NP_059989.3:p.Thr1663Ala