Canonical Allele Identifier: CA366234091

Gene: ARID1B

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3808A>C	ENSP00000055163.8:p.Ser1270Arg
ENST00000414678.8:c.3877A>C	ENSP00000412835.3:p.Ser1293Arg
ENST00000637015.2:c.4096A>C	ENSP00000489729.2:p.Ser1366Arg
ENST00000346085.10:c.3847A>C	ENSP00000344546.5:p.Ser1283Arg
ENST00000350026.10:c.3559A>C	ENSP00000055163.7:p.Ser1187Arg
ENST00000414678.7:c.2125A>C	ENSP00000412835.2:p.Ser709Arg
ENST00000635849.1:c.1288A>C	ENSP00000490948.1:p.Ser430Arg
ENST00000635957.1:c.922A>C	ENSP00000490385.1:p.Ser308Arg
ENST00000636930.2:c.3967A>C MANE Select	ENSP00000490491.2:p.Ser1323Arg
ENST00000636940.1:n.1964A>C
ENST00000637015.1:c.1335A>C
ENST00000637568.1:c.1249A>C
ENST00000637741.1:n.633A>C
ENST00000637810.1:c.1309A>C	ENSP00000489636.1:p.Ser437Arg
ENST00000637904.1:c.1468A>C	ENSP00000490550.1:p.Ser490Arg
ENST00000647938.1:c.3598A>C	ENSP00000498155.1:p.Ser1200Arg
ENST00000346085.9:c.3598A>C	ENSP00000344546.4:p.Ser1200Arg
ENST00000350026.9:c.3559A>C	ENSP00000055163.7:p.Ser1187Arg
ENST00000414678.6:c.2125A>C	ENSP00000412835.2:p.Ser709Arg
NM_017519.2:c.3559A>C	NP_059989.2:p.Ser1187Arg
NM_020732.3:c.3598A>C	NP_065783.3:p.Ser1200Arg
XM_005267069.3:c.3718A>C	XP_005267126.2:p.Ser1240Arg
XM_011535984.1:c.2797A>C	XP_011534286.1:p.Ser933Arg
XM_011535985.1:c.2617A>C	XP_011534287.1:p.Ser873Arg
XM_011535986.1:c.2377A>C	XP_011534288.1:p.Ser793Arg
XM_011535987.1:c.1996A>C	XP_011534289.1:p.Ser666Arg
XM_011535988.1:c.859A>C	XP_011534290.1:p.Ser287Arg
NM_001346813.1:c.3718A>C	NP_001333742.1:p.Ser1240Arg
NM_001363725.1:c.1468A>C	NP_001350654.1:p.Ser490Arg
XM_011535984.2:c.3928A>C	XP_011534286.2:p.Ser1310Arg
XM_011535988.3:c.859A>C	XP_011534290.1:p.Ser287Arg
XM_017011103.2:c.3829A>C	XP_016866592.1:p.Ser1277Arg
XM_017011104.1:c.3799A>C	XP_016866593.1:p.Ser1267Arg
XM_017011105.2:c.3769A>C	XP_016866594.1:p.Ser1257Arg
XM_017011106.2:c.3640A>C	XP_016866595.1:p.Ser1214Arg
XM_017011107.2:c.3619A>C	XP_016866596.1:p.Ser1207Arg
XR_002956289.1:n.4011A>C
NM_001363725.2:c.1468A>C	NP_001350654.1:p.Ser490Arg
NM_001371656.1:c.3847A>C	NP_001358585.1:p.Ser1283Arg
NM_001374820.1:c.3847A>C	NP_001361749.1:p.Ser1283Arg
NM_001374828.1:c.3967A>C MANE Select	NP_001361757.1:p.Ser1323Arg
NM_017519.3:c.3808A>C	NP_059989.3:p.Ser1270Arg