Canonical Allele Identifier: CA366228120

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128317496
• MyVariant Identifiers: chr6:g.157502250A>G (hg19) ; chr6:g.157181116A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181116A>G , CM000668.2:g.157181116A>G	GRCh38
NC_000006.11:g.157502250A>G , CM000668.1:g.157502250A>G	GRCh37
NC_000006.10:g.157543942A>G	NCBI36
NG_032093.1:g.408187A>G
NG_032093.2:g.408187A>G
NG_066624.1:g.410091A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3493A>G	ENSP00000055163.8:p.Lys1165Glu
ENST00000414678.8:c.3562A>G	ENSP00000412835.3:p.Lys1188Glu
ENST00000637015.2:c.3781A>G	ENSP00000489729.2:p.Lys1261Glu
ENST00000319584.11:c.1666A>G	ENSP00000313006.7:p.Lys556Glu
ENST00000346085.10:c.3532A>G	ENSP00000344546.5:p.Lys1178Glu
ENST00000350026.10:c.3244A>G	ENSP00000055163.7:p.Lys1082Glu
ENST00000414678.7:c.1810A>G	ENSP00000412835.2:p.Lys604Glu
ENST00000635849.1:c.973A>G	ENSP00000490948.1:p.Lys325Glu
ENST00000635957.1:c.607A>G	ENSP00000490385.1:p.Lys203Glu
ENST00000636930.2:c.3652A>G MANE Select	ENSP00000490491.2:p.Lys1218Glu
ENST00000636940.1:n.1649A>G
ENST00000637015.1:c.1020A>G
ENST00000637568.1:c.934A>G
ENST00000637741.1:n.318A>G
ENST00000637810.1:c.994A>G	ENSP00000489636.1:p.Lys332Glu
ENST00000637904.1:c.1153A>G	ENSP00000490550.1:p.Lys385Glu
ENST00000647938.1:c.3283A>G	ENSP00000498155.1:p.Lys1095Glu
ENST00000319584.10:c.1669A>G	ENSP00000313006.6:p.Lys557Glu
ENST00000346085.9:c.3283A>G	ENSP00000344546.4:p.Lys1095Glu
ENST00000350026.9:c.3244A>G	ENSP00000055163.7:p.Lys1082Glu
ENST00000400790.3:c.445A>G	ENSP00000383596.3:p.Lys149Glu
ENST00000414678.6:c.1810A>G	ENSP00000412835.2:p.Lys604Glu
ENST00000478761.3:c.854A>G
NM_017519.2:c.3244A>G	NP_059989.2:p.Lys1082Glu
NM_020732.3:c.3283A>G	NP_065783.3:p.Lys1095Glu
XM_005267069.3:c.3403A>G	XP_005267126.2:p.Lys1135Glu
XM_011535984.1:c.2482A>G	XP_011534286.1:p.Lys828Glu
XM_011535985.1:c.2302A>G	XP_011534287.1:p.Lys768Glu
XM_011535986.1:c.2062A>G	XP_011534288.1:p.Lys688Glu
XM_011535987.1:c.1681A>G	XP_011534289.1:p.Lys561Glu
XM_011535988.1:c.544A>G	XP_011534290.1:p.Lys182Glu
NM_001346813.1:c.3403A>G	NP_001333742.1:p.Lys1135Glu
NM_001363725.1:c.1153A>G	NP_001350654.1:p.Lys385Glu
XM_011535984.2:c.3613A>G	XP_011534286.2:p.Lys1205Glu
XM_011535988.3:c.544A>G	XP_011534290.1:p.Lys182Glu
XM_017011103.2:c.3514A>G	XP_016866592.1:p.Lys1172Glu
XM_017011104.1:c.3484A>G	XP_016866593.1:p.Lys1162Glu
XM_017011105.2:c.3454A>G	XP_016866594.1:p.Lys1152Glu
XM_017011106.2:c.3325A>G	XP_016866595.1:p.Lys1109Glu
XM_017011107.2:c.3304A>G	XP_016866596.1:p.Lys1102Glu
XR_002956289.1:n.3696A>G
NM_001363725.2:c.1153A>G	NP_001350654.1:p.Lys385Glu
NM_001371656.1:c.3532A>G	NP_001358585.1:p.Lys1178Glu
NM_001374820.1:c.3532A>G	NP_001361749.1:p.Lys1178Glu
NM_001374828.1:c.3652A>G MANE Select	NP_001361757.1:p.Lys1218Glu
NM_017519.3:c.3493A>G	NP_059989.3:p.Lys1165Glu