Canonical Allele Identifier: CA366242787

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128376332
• MyVariant Identifiers: chr6:g.157522505A>T (hg19) ; chr6:g.157201371A>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4987A>T	ENSP00000055163.8:p.Thr1663Ser
ENST00000414678.8:c.5056A>T	ENSP00000412835.3:p.Thr1686Ser
ENST00000637015.2:c.5275A>T	ENSP00000489729.2:p.Thr1759Ser
ENST00000346085.10:c.5026A>T	ENSP00000344546.5:p.Thr1676Ser
ENST00000350026.10:c.4738A>T	ENSP00000055163.7:p.Thr1580Ser
ENST00000414678.7:c.3304A>T	ENSP00000412835.2:p.Thr1102Ser
ENST00000635849.1:c.2467A>T	ENSP00000490948.1:p.Thr823Ser
ENST00000635957.1:c.2098A>T	ENSP00000490385.1:p.Thr700Ser
ENST00000636227.1:n.3609A>T
ENST00000636254.1:n.1066A>T
ENST00000636930.2:c.5146A>T MANE Select	ENSP00000490491.2:p.Thr1716Ser
ENST00000636940.1:n.3143A>T
ENST00000637015.1:c.2514A>T
ENST00000637568.1:c.2428A>T
ENST00000637741.1:n.1812A>T
ENST00000637810.1:c.2488A>T	ENSP00000489636.1:p.Thr830Ser
ENST00000637904.1:c.2647A>T	ENSP00000490550.1:p.Thr883Ser
ENST00000647938.1:c.4777A>T	ENSP00000498155.1:p.Thr1593Ser
ENST00000346085.9:c.4777A>T	ENSP00000344546.4:p.Thr1593Ser
ENST00000350026.9:c.4738A>T	ENSP00000055163.7:p.Thr1580Ser
ENST00000414678.6:c.3304A>T	ENSP00000412835.2:p.Thr1102Ser
NM_017519.2:c.4738A>T	NP_059989.2:p.Thr1580Ser
NM_020732.3:c.4777A>T	NP_065783.3:p.Thr1593Ser
XM_005267069.3:c.4897A>T	XP_005267126.2:p.Thr1633Ser
XM_011535984.1:c.3976A>T	XP_011534286.1:p.Thr1326Ser
XM_011535985.1:c.3796A>T	XP_011534287.1:p.Thr1266Ser
XM_011535986.1:c.3556A>T	XP_011534288.1:p.Thr1186Ser
XM_011535987.1:c.3175A>T	XP_011534289.1:p.Thr1059Ser
XM_011535988.1:c.2038A>T	XP_011534290.1:p.Thr680Ser
NM_001346813.1:c.4897A>T	NP_001333742.1:p.Thr1633Ser
NM_001363725.1:c.2647A>T	NP_001350654.1:p.Thr883Ser
XM_011535984.2:c.5107A>T	XP_011534286.2:p.Thr1703Ser
XM_011535988.3:c.2038A>T	XP_011534290.1:p.Thr680Ser
XM_017011103.2:c.5008A>T	XP_016866592.1:p.Thr1670Ser
XM_017011104.1:c.4978A>T	XP_016866593.1:p.Thr1660Ser
XM_017011105.2:c.4948A>T	XP_016866594.1:p.Thr1650Ser
XM_017011106.2:c.4819A>T	XP_016866595.1:p.Thr1607Ser
XM_017011107.2:c.4798A>T	XP_016866596.1:p.Thr1600Ser
XR_002956289.1:n.5093A>T
NM_001363725.2:c.2647A>T	NP_001350654.1:p.Thr883Ser
NM_001371656.1:c.5026A>T	NP_001358585.1:p.Thr1676Ser
NM_001374820.1:c.5026A>T	NP_001361749.1:p.Thr1676Ser
NM_001374828.1:c.5146A>T MANE Select	NP_001361757.1:p.Thr1716Ser
NM_017519.3:c.4987A>T	NP_059989.3:p.Thr1663Ser