Canonical Allele Identifier: CA366242944

Gene: ARID1B

Linked Data

• dbSNP Id: rs971931551
• MyVariant Identifiers: chr6:g.157522536G>T (hg19) ; chr6:g.157201402G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201402G>T , CM000668.2:g.157201402G>T	GRCh38
NC_000006.11:g.157522536G>T , CM000668.1:g.157522536G>T	GRCh37
NC_000006.10:g.157564228G>T	NCBI36
NG_032093.1:g.428473G>T
NG_032093.2:g.428473G>T
NG_066624.1:g.430377G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.5018G>T	ENSP00000055163.8:p.Arg1673Ile
ENST00000414678.8:c.5087G>T	ENSP00000412835.3:p.Arg1696Ile
ENST00000637015.2:c.5306G>T	ENSP00000489729.2:p.Arg1769Ile
ENST00000346085.10:c.5057G>T	ENSP00000344546.5:p.Arg1686Ile
ENST00000350026.10:c.4769G>T	ENSP00000055163.7:p.Arg1590Ile
ENST00000414678.7:c.3335G>T	ENSP00000412835.2:p.Arg1112Ile
ENST00000635849.1:c.2498G>T	ENSP00000490948.1:p.Arg833Ile
ENST00000635957.1:c.2129G>T	ENSP00000490385.1:p.Arg710Ile
ENST00000636227.1:n.3640G>T
ENST00000636254.1:n.1097G>T
ENST00000636930.2:c.5177G>T MANE Select	ENSP00000490491.2:p.Arg1726Ile
ENST00000636940.1:n.3174G>T
ENST00000637015.1:c.2545G>T
ENST00000637568.1:c.2459G>T
ENST00000637741.1:n.1843G>T
ENST00000637810.1:c.2519G>T	ENSP00000489636.1:p.Arg840Ile
ENST00000637904.1:c.2678G>T	ENSP00000490550.1:p.Arg893Ile
ENST00000647938.1:c.4808G>T	ENSP00000498155.1:p.Arg1603Ile
ENST00000346085.9:c.4808G>T	ENSP00000344546.4:p.Arg1603Ile
ENST00000350026.9:c.4769G>T	ENSP00000055163.7:p.Arg1590Ile
ENST00000414678.6:c.3335G>T	ENSP00000412835.2:p.Arg1112Ile
NM_017519.2:c.4769G>T	NP_059989.2:p.Arg1590Ile
NM_020732.3:c.4808G>T	NP_065783.3:p.Arg1603Ile
XM_005267069.3:c.4928G>T	XP_005267126.2:p.Arg1643Ile
XM_011535984.1:c.4007G>T	XP_011534286.1:p.Arg1336Ile
XM_011535985.1:c.3827G>T	XP_011534287.1:p.Arg1276Ile
XM_011535986.1:c.3587G>T	XP_011534288.1:p.Arg1196Ile
XM_011535987.1:c.3206G>T	XP_011534289.1:p.Arg1069Ile
XM_011535988.1:c.2069G>T	XP_011534290.1:p.Arg690Ile
NM_001346813.1:c.4928G>T	NP_001333742.1:p.Arg1643Ile
NM_001363725.1:c.2678G>T	NP_001350654.1:p.Arg893Ile
XM_011535984.2:c.5138G>T	XP_011534286.2:p.Arg1713Ile
XM_011535988.3:c.2069G>T	XP_011534290.1:p.Arg690Ile
XM_017011103.2:c.5039G>T	XP_016866592.1:p.Arg1680Ile
XM_017011104.1:c.5009G>T	XP_016866593.1:p.Arg1670Ile
XM_017011105.2:c.4979G>T	XP_016866594.1:p.Arg1660Ile
XM_017011106.2:c.4850G>T	XP_016866595.1:p.Arg1617Ile
XM_017011107.2:c.4829G>T	XP_016866596.1:p.Arg1610Ile
XR_002956289.1:n.5124G>T
NM_001363725.2:c.2678G>T	NP_001350654.1:p.Arg893Ile
NM_001371656.1:c.5057G>T	NP_001358585.1:p.Arg1686Ile
NM_001374820.1:c.5057G>T	NP_001361749.1:p.Arg1686Ile
NM_001374828.1:c.5177G>T MANE Select	NP_001361757.1:p.Arg1726Ile
NM_017519.3:c.5018G>T	NP_059989.3:p.Arg1673Ile