Canonical Allele Identifier: CA366242955

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128376606
• MyVariant Identifiers: chr6:g.157522538A>T (hg19) ; chr6:g.157201404A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201404A>T , CM000668.2:g.157201404A>T	GRCh38
NC_000006.11:g.157522538A>T , CM000668.1:g.157522538A>T	GRCh37
NC_000006.10:g.157564230A>T	NCBI36
NG_032093.1:g.428475A>T
NG_032093.2:g.428475A>T
NG_066624.1:g.430379A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.5020A>T	ENSP00000055163.8:p.Arg1674Trp
ENST00000414678.8:c.5089A>T	ENSP00000412835.3:p.Arg1697Trp
ENST00000637015.2:c.5308A>T	ENSP00000489729.2:p.Arg1770Trp
ENST00000346085.10:c.5059A>T	ENSP00000344546.5:p.Arg1687Trp
ENST00000350026.10:c.4771A>T	ENSP00000055163.7:p.Arg1591Trp
ENST00000414678.7:c.3337A>T	ENSP00000412835.2:p.Arg1113Trp
ENST00000635849.1:c.2500A>T	ENSP00000490948.1:p.Arg834Trp
ENST00000635957.1:c.2131A>T	ENSP00000490385.1:p.Arg711Trp
ENST00000636227.1:n.3642A>T
ENST00000636254.1:n.1099A>T
ENST00000636930.2:c.5179A>T MANE Select	ENSP00000490491.2:p.Arg1727Trp
ENST00000636940.1:n.3176A>T
ENST00000637015.1:c.2547A>T
ENST00000637568.1:c.2461A>T
ENST00000637741.1:n.1845A>T
ENST00000637810.1:c.2521A>T	ENSP00000489636.1:p.Arg841Trp
ENST00000637904.1:c.2680A>T	ENSP00000490550.1:p.Arg894Trp
ENST00000647938.1:c.4810A>T	ENSP00000498155.1:p.Arg1604Trp
ENST00000346085.9:c.4810A>T	ENSP00000344546.4:p.Arg1604Trp
ENST00000350026.9:c.4771A>T	ENSP00000055163.7:p.Arg1591Trp
ENST00000414678.6:c.3337A>T	ENSP00000412835.2:p.Arg1113Trp
NM_017519.2:c.4771A>T	NP_059989.2:p.Arg1591Trp
NM_020732.3:c.4810A>T	NP_065783.3:p.Arg1604Trp
XM_005267069.3:c.4930A>T	XP_005267126.2:p.Arg1644Trp
XM_011535984.1:c.4009A>T	XP_011534286.1:p.Arg1337Trp
XM_011535985.1:c.3829A>T	XP_011534287.1:p.Arg1277Trp
XM_011535986.1:c.3589A>T	XP_011534288.1:p.Arg1197Trp
XM_011535987.1:c.3208A>T	XP_011534289.1:p.Arg1070Trp
XM_011535988.1:c.2071A>T	XP_011534290.1:p.Arg691Trp
NM_001346813.1:c.4930A>T	NP_001333742.1:p.Arg1644Trp
NM_001363725.1:c.2680A>T	NP_001350654.1:p.Arg894Trp
XM_011535984.2:c.5140A>T	XP_011534286.2:p.Arg1714Trp
XM_011535988.3:c.2071A>T	XP_011534290.1:p.Arg691Trp
XM_017011103.2:c.5041A>T	XP_016866592.1:p.Arg1681Trp
XM_017011104.1:c.5011A>T	XP_016866593.1:p.Arg1671Trp
XM_017011105.2:c.4981A>T	XP_016866594.1:p.Arg1661Trp
XM_017011106.2:c.4852A>T	XP_016866595.1:p.Arg1618Trp
XM_017011107.2:c.4831A>T	XP_016866596.1:p.Arg1611Trp
XR_002956289.1:n.5126A>T
NM_001363725.2:c.2680A>T	NP_001350654.1:p.Arg894Trp
NM_001371656.1:c.5059A>T	NP_001358585.1:p.Arg1687Trp
NM_001374820.1:c.5059A>T	NP_001361749.1:p.Arg1687Trp
NM_001374828.1:c.5179A>T MANE Select	NP_001361757.1:p.Arg1727Trp
NM_017519.3:c.5020A>T	NP_059989.3:p.Arg1674Trp