Canonical Allele Identifier: CA452783987

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128366608
• MyVariant Identifiers: chr6:g.157520026G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157198892G>C , CM000668.2:g.157198892G>C	GRCh38
NC_000006.11:g.157520026G>C , CM000668.1:g.157520026G>C	GRCh37
NC_000006.10:g.157561718G>C	NCBI36
NG_032093.1:g.425963G>C
NG_032093.2:g.425963G>C
NG_066624.1:g.427867G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4305G>C	ENSP00000055163.8:p.Leu1435=
ENST00000414678.8:c.4374G>C	ENSP00000412835.3:p.Leu1458=
ENST00000637015.2:c.4593G>C	ENSP00000489729.2:p.Leu1531=
ENST00000346085.10:c.4344G>C	ENSP00000344546.5:p.Leu1448=
ENST00000350026.10:c.4056G>C	ENSP00000055163.7:p.Leu1352=
ENST00000414678.7:c.2622G>C	ENSP00000412835.2:p.Leu874=
ENST00000635849.1:c.1785G>C	ENSP00000490948.1:p.Leu595=
ENST00000635957.1:c.1416G>C	ENSP00000490385.1:p.Leu472=
ENST00000636227.1:n.2927G>C
ENST00000636254.1:n.384G>C
ENST00000636930.2:c.4464G>C MANE Select	ENSP00000490491.2:p.Leu1488=
ENST00000636940.1:n.2461G>C
ENST00000637015.1:c.1832G>C
ENST00000637568.1:c.1746G>C
ENST00000637741.1:n.1130G>C
ENST00000637810.1:c.1806G>C	ENSP00000489636.1:p.Leu602=
ENST00000637904.1:c.1965G>C	ENSP00000490550.1:p.Leu655=
ENST00000647938.1:c.4095G>C	ENSP00000498155.1:p.Leu1365=
ENST00000346085.9:c.4095G>C	ENSP00000344546.4:p.Leu1365=
ENST00000350026.9:c.4056G>C	ENSP00000055163.7:p.Leu1352=
ENST00000414678.6:c.2622G>C	ENSP00000412835.2:p.Leu874=
NM_017519.2:c.4056G>C	NP_059989.2:p.Leu1352=
NM_020732.3:c.4095G>C	NP_065783.3:p.Leu1365=
XM_005267069.3:c.4215G>C	XP_005267126.2:p.Leu1405=
XM_011535984.1:c.3294G>C	XP_011534286.1:p.Leu1098=
XM_011535985.1:c.3114G>C	XP_011534287.1:p.Leu1038=
XM_011535986.1:c.2874G>C	XP_011534288.1:p.Leu958=
XM_011535987.1:c.2493G>C	XP_011534289.1:p.Leu831=
XM_011535988.1:c.1356G>C	XP_011534290.1:p.Leu452=
NM_001346813.1:c.4215G>C	NP_001333742.1:p.Leu1405=
NM_001363725.1:c.1965G>C	NP_001350654.1:p.Leu655=
XM_011535984.2:c.4425G>C	XP_011534286.2:p.Leu1475=
XM_011535988.3:c.1356G>C	XP_011534290.1:p.Leu452=
XM_017011103.2:c.4326G>C	XP_016866592.1:p.Leu1442=
XM_017011104.1:c.4296G>C	XP_016866593.1:p.Leu1432=
XM_017011105.2:c.4266G>C	XP_016866594.1:p.Leu1422=
XM_017011106.2:c.4137G>C	XP_016866595.1:p.Leu1379=
XM_017011107.2:c.4116G>C	XP_016866596.1:p.Leu1372=
XR_002956289.1:n.4427-1813G>C
NM_001363725.2:c.1965G>C	NP_001350654.1:p.Leu655=
NM_001371656.1:c.4344G>C	NP_001358585.1:p.Leu1448=
NM_001374820.1:c.4344G>C	NP_001361749.1:p.Leu1448=
NM_001374828.1:c.4464G>C MANE Select	NP_001361757.1:p.Leu1488=
NM_017519.3:c.4305G>C	NP_059989.3:p.Leu1435=