Canonical Allele Identifier: CA366228232

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157502266T>G (hg19) ; chr6:g.157181132T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181132T>G , CM000668.2:g.157181132T>G	GRCh38
NC_000006.11:g.157502266T>G , CM000668.1:g.157502266T>G	GRCh37
NC_000006.10:g.157543958T>G	NCBI36
NG_032093.1:g.408203T>G
NG_032093.2:g.408203T>G
NG_066624.1:g.410107T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3509T>G	ENSP00000055163.8:p.Leu1170Arg
ENST00000414678.8:c.3578T>G	ENSP00000412835.3:p.Leu1193Arg
ENST00000637015.2:c.3797T>G	ENSP00000489729.2:p.Leu1266Arg
ENST00000319584.11:c.1682T>G	ENSP00000313006.7:p.Leu561Arg
ENST00000346085.10:c.3548T>G	ENSP00000344546.5:p.Leu1183Arg
ENST00000350026.10:c.3260T>G	ENSP00000055163.7:p.Leu1087Arg
ENST00000414678.7:c.1826T>G	ENSP00000412835.2:p.Leu609Arg
ENST00000635849.1:c.989T>G	ENSP00000490948.1:p.Leu330Arg
ENST00000635957.1:c.623T>G	ENSP00000490385.1:p.Leu208Arg
ENST00000636930.2:c.3668T>G MANE Select	ENSP00000490491.2:p.Leu1223Arg
ENST00000636940.1:n.1665T>G
ENST00000637015.1:c.1036T>G
ENST00000637568.1:c.950T>G
ENST00000637741.1:n.334T>G
ENST00000637810.1:c.1010T>G	ENSP00000489636.1:p.Leu337Arg
ENST00000637904.1:c.1169T>G	ENSP00000490550.1:p.Leu390Arg
ENST00000647938.1:c.3299T>G	ENSP00000498155.1:p.Leu1100Arg
ENST00000319584.10:c.1685T>G	ENSP00000313006.6:p.Leu562Arg
ENST00000346085.9:c.3299T>G	ENSP00000344546.4:p.Leu1100Arg
ENST00000350026.9:c.3260T>G	ENSP00000055163.7:p.Leu1087Arg
ENST00000400790.3:c.461T>G	ENSP00000383596.3:p.Leu154Arg
ENST00000414678.6:c.1826T>G	ENSP00000412835.2:p.Leu609Arg
ENST00000478761.3:c.870T>G
NM_017519.2:c.3260T>G	NP_059989.2:p.Leu1087Arg
NM_020732.3:c.3299T>G	NP_065783.3:p.Leu1100Arg
XM_005267069.3:c.3419T>G	XP_005267126.2:p.Leu1140Arg
XM_011535984.1:c.2498T>G	XP_011534286.1:p.Leu833Arg
XM_011535985.1:c.2318T>G	XP_011534287.1:p.Leu773Arg
XM_011535986.1:c.2078T>G	XP_011534288.1:p.Leu693Arg
XM_011535987.1:c.1697T>G	XP_011534289.1:p.Leu566Arg
XM_011535988.1:c.560T>G	XP_011534290.1:p.Leu187Arg
NM_001346813.1:c.3419T>G	NP_001333742.1:p.Leu1140Arg
NM_001363725.1:c.1169T>G	NP_001350654.1:p.Leu390Arg
XM_011535984.2:c.3629T>G	XP_011534286.2:p.Leu1210Arg
XM_011535988.3:c.560T>G	XP_011534290.1:p.Leu187Arg
XM_017011103.2:c.3530T>G	XP_016866592.1:p.Leu1177Arg
XM_017011104.1:c.3500T>G	XP_016866593.1:p.Leu1167Arg
XM_017011105.2:c.3470T>G	XP_016866594.1:p.Leu1157Arg
XM_017011106.2:c.3341T>G	XP_016866595.1:p.Leu1114Arg
XM_017011107.2:c.3320T>G	XP_016866596.1:p.Leu1107Arg
XR_002956289.1:n.3712T>G
NM_001363725.2:c.1169T>G	NP_001350654.1:p.Leu390Arg
NM_001371656.1:c.3548T>G	NP_001358585.1:p.Leu1183Arg
NM_001374820.1:c.3548T>G	NP_001361749.1:p.Leu1183Arg
NM_001374828.1:c.3668T>G MANE Select	NP_001361757.1:p.Leu1223Arg
NM_017519.3:c.3509T>G	NP_059989.3:p.Leu1170Arg