Canonical Allele Identifier: CA366234090

Gene: ARID1B

Linked Data

• gnomAD v4: 6-157189689-A-G
• MyVariant Identifiers: chr6:g.157510823A>G (hg19) ; chr6:g.157189689A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189689A>G , CM000668.2:g.157189689A>G	GRCh38
NC_000006.11:g.157510823A>G , CM000668.1:g.157510823A>G	GRCh37
NC_000006.10:g.157552515A>G	NCBI36
NG_032093.1:g.416760A>G
NG_032093.2:g.416760A>G
NG_066624.1:g.418664A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3808A>G	ENSP00000055163.8:p.Ser1270Gly
ENST00000414678.8:c.3877A>G	ENSP00000412835.3:p.Ser1293Gly
ENST00000637015.2:c.4096A>G	ENSP00000489729.2:p.Ser1366Gly
ENST00000346085.10:c.3847A>G	ENSP00000344546.5:p.Ser1283Gly
ENST00000350026.10:c.3559A>G	ENSP00000055163.7:p.Ser1187Gly
ENST00000414678.7:c.2125A>G	ENSP00000412835.2:p.Ser709Gly
ENST00000635849.1:c.1288A>G	ENSP00000490948.1:p.Ser430Gly
ENST00000635957.1:c.922A>G	ENSP00000490385.1:p.Ser308Gly
ENST00000636930.2:c.3967A>G MANE Select	ENSP00000490491.2:p.Ser1323Gly
ENST00000636940.1:n.1964A>G
ENST00000637015.1:c.1335A>G
ENST00000637568.1:c.1249A>G
ENST00000637741.1:n.633A>G
ENST00000637810.1:c.1309A>G	ENSP00000489636.1:p.Ser437Gly
ENST00000637904.1:c.1468A>G	ENSP00000490550.1:p.Ser490Gly
ENST00000647938.1:c.3598A>G	ENSP00000498155.1:p.Ser1200Gly
ENST00000346085.9:c.3598A>G	ENSP00000344546.4:p.Ser1200Gly
ENST00000350026.9:c.3559A>G	ENSP00000055163.7:p.Ser1187Gly
ENST00000414678.6:c.2125A>G	ENSP00000412835.2:p.Ser709Gly
NM_017519.2:c.3559A>G	NP_059989.2:p.Ser1187Gly
NM_020732.3:c.3598A>G	NP_065783.3:p.Ser1200Gly
XM_005267069.3:c.3718A>G	XP_005267126.2:p.Ser1240Gly
XM_011535984.1:c.2797A>G	XP_011534286.1:p.Ser933Gly
XM_011535985.1:c.2617A>G	XP_011534287.1:p.Ser873Gly
XM_011535986.1:c.2377A>G	XP_011534288.1:p.Ser793Gly
XM_011535987.1:c.1996A>G	XP_011534289.1:p.Ser666Gly
XM_011535988.1:c.859A>G	XP_011534290.1:p.Ser287Gly
NM_001346813.1:c.3718A>G	NP_001333742.1:p.Ser1240Gly
NM_001363725.1:c.1468A>G	NP_001350654.1:p.Ser490Gly
XM_011535984.2:c.3928A>G	XP_011534286.2:p.Ser1310Gly
XM_011535988.3:c.859A>G	XP_011534290.1:p.Ser287Gly
XM_017011103.2:c.3829A>G	XP_016866592.1:p.Ser1277Gly
XM_017011104.1:c.3799A>G	XP_016866593.1:p.Ser1267Gly
XM_017011105.2:c.3769A>G	XP_016866594.1:p.Ser1257Gly
XM_017011106.2:c.3640A>G	XP_016866595.1:p.Ser1214Gly
XM_017011107.2:c.3619A>G	XP_016866596.1:p.Ser1207Gly
XR_002956289.1:n.4011A>G
NM_001363725.2:c.1468A>G	NP_001350654.1:p.Ser490Gly
NM_001371656.1:c.3847A>G	NP_001358585.1:p.Ser1283Gly
NM_001374820.1:c.3847A>G	NP_001361749.1:p.Ser1283Gly
NM_001374828.1:c.3967A>G MANE Select	NP_001361757.1:p.Ser1323Gly
NM_017519.3:c.3808A>G	NP_059989.3:p.Ser1270Gly