Canonical Allele Identifier: CA366242934

Gene: ARID1B

Linked Data

• dbSNP Id: rs1252161880
• MyVariant Identifiers: chr6:g.157522535A>T (hg19) ; chr6:g.157201401A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201401A>T , CM000668.2:g.157201401A>T	GRCh38
NC_000006.11:g.157522535A>T , CM000668.1:g.157522535A>T	GRCh37
NC_000006.10:g.157564227A>T	NCBI36
NG_032093.1:g.428472A>T
NG_032093.2:g.428472A>T
NG_066624.1:g.430376A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.5017A>T	ENSP00000055163.8:p.Arg1673Ter
ENST00000414678.8:c.5086A>T	ENSP00000412835.3:p.Arg1696Ter
ENST00000637015.2:c.5305A>T	ENSP00000489729.2:p.Arg1769Ter
ENST00000346085.10:c.5056A>T	ENSP00000344546.5:p.Arg1686Ter
ENST00000350026.10:c.4768A>T	ENSP00000055163.7:p.Arg1590Ter
ENST00000414678.7:c.3334A>T	ENSP00000412835.2:p.Arg1112Ter
ENST00000635849.1:c.2497A>T	ENSP00000490948.1:p.Arg833Ter
ENST00000635957.1:c.2128A>T	ENSP00000490385.1:p.Arg710Ter
ENST00000636227.1:n.3639A>T
ENST00000636254.1:n.1096A>T
ENST00000636930.2:c.5176A>T MANE Select	ENSP00000490491.2:p.Arg1726Ter
ENST00000636940.1:n.3173A>T
ENST00000637015.1:c.2544A>T
ENST00000637568.1:c.2458A>T
ENST00000637741.1:n.1842A>T
ENST00000637810.1:c.2518A>T	ENSP00000489636.1:p.Arg840Ter
ENST00000637904.1:c.2677A>T	ENSP00000490550.1:p.Arg893Ter
ENST00000647938.1:c.4807A>T	ENSP00000498155.1:p.Arg1603Ter
ENST00000346085.9:c.4807A>T	ENSP00000344546.4:p.Arg1603Ter
ENST00000350026.9:c.4768A>T	ENSP00000055163.7:p.Arg1590Ter
ENST00000414678.6:c.3334A>T	ENSP00000412835.2:p.Arg1112Ter
NM_017519.2:c.4768A>T	NP_059989.2:p.Arg1590Ter
NM_020732.3:c.4807A>T	NP_065783.3:p.Arg1603Ter
XM_005267069.3:c.4927A>T	XP_005267126.2:p.Arg1643Ter
XM_011535984.1:c.4006A>T	XP_011534286.1:p.Arg1336Ter
XM_011535985.1:c.3826A>T	XP_011534287.1:p.Arg1276Ter
XM_011535986.1:c.3586A>T	XP_011534288.1:p.Arg1196Ter
XM_011535987.1:c.3205A>T	XP_011534289.1:p.Arg1069Ter
XM_011535988.1:c.2068A>T	XP_011534290.1:p.Arg690Ter
NM_001346813.1:c.4927A>T	NP_001333742.1:p.Arg1643Ter
NM_001363725.1:c.2677A>T	NP_001350654.1:p.Arg893Ter
XM_011535984.2:c.5137A>T	XP_011534286.2:p.Arg1713Ter
XM_011535988.3:c.2068A>T	XP_011534290.1:p.Arg690Ter
XM_017011103.2:c.5038A>T	XP_016866592.1:p.Arg1680Ter
XM_017011104.1:c.5008A>T	XP_016866593.1:p.Arg1670Ter
XM_017011105.2:c.4978A>T	XP_016866594.1:p.Arg1660Ter
XM_017011106.2:c.4849A>T	XP_016866595.1:p.Arg1617Ter
XM_017011107.2:c.4828A>T	XP_016866596.1:p.Arg1610Ter
XR_002956289.1:n.5123A>T
NM_001363725.2:c.2677A>T	NP_001350654.1:p.Arg893Ter
NM_001371656.1:c.5056A>T	NP_001358585.1:p.Arg1686Ter
NM_001374820.1:c.5056A>T	NP_001361749.1:p.Arg1686Ter
NM_001374828.1:c.5176A>T MANE Select	NP_001361757.1:p.Arg1726Ter
NM_017519.3:c.5017A>T	NP_059989.3:p.Arg1673Ter