Canonical Allele Identifier: CA366242442

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128375793
• MyVariant Identifiers: chr6:g.157522437G>C (hg19) ; chr6:g.157201303G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201303G>C , CM000668.2:g.157201303G>C	GRCh38
NC_000006.11:g.157522437G>C , CM000668.1:g.157522437G>C	GRCh37
NC_000006.10:g.157564129G>C	NCBI36
NG_032093.1:g.428374G>C
NG_032093.2:g.428374G>C
NG_066624.1:g.430278G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4919G>C	ENSP00000055163.8:p.Ser1640Thr
ENST00000414678.8:c.4988G>C	ENSP00000412835.3:p.Ser1663Thr
ENST00000637015.2:c.5207G>C	ENSP00000489729.2:p.Ser1736Thr
ENST00000346085.10:c.4958G>C	ENSP00000344546.5:p.Ser1653Thr
ENST00000350026.10:c.4670G>C	ENSP00000055163.7:p.Ser1557Thr
ENST00000414678.7:c.3236G>C	ENSP00000412835.2:p.Ser1079Thr
ENST00000635849.1:c.2399G>C	ENSP00000490948.1:p.Ser800Thr
ENST00000635957.1:c.2030G>C	ENSP00000490385.1:p.Ser677Thr
ENST00000636227.1:n.3541G>C
ENST00000636254.1:n.998G>C
ENST00000636930.2:c.5078G>C MANE Select	ENSP00000490491.2:p.Ser1693Thr
ENST00000636940.1:n.3075G>C
ENST00000637015.1:c.2446G>C
ENST00000637568.1:c.2360G>C
ENST00000637741.1:n.1744G>C
ENST00000637810.1:c.2420G>C	ENSP00000489636.1:p.Ser807Thr
ENST00000637904.1:c.2579G>C	ENSP00000490550.1:p.Ser860Thr
ENST00000647938.1:c.4709G>C	ENSP00000498155.1:p.Ser1570Thr
ENST00000346085.9:c.4709G>C	ENSP00000344546.4:p.Ser1570Thr
ENST00000350026.9:c.4670G>C	ENSP00000055163.7:p.Ser1557Thr
ENST00000414678.6:c.3236G>C	ENSP00000412835.2:p.Ser1079Thr
NM_017519.2:c.4670G>C	NP_059989.2:p.Ser1557Thr
NM_020732.3:c.4709G>C	NP_065783.3:p.Ser1570Thr
XM_005267069.3:c.4829G>C	XP_005267126.2:p.Ser1610Thr
XM_011535984.1:c.3908G>C	XP_011534286.1:p.Ser1303Thr
XM_011535985.1:c.3728G>C	XP_011534287.1:p.Ser1243Thr
XM_011535986.1:c.3488G>C	XP_011534288.1:p.Ser1163Thr
XM_011535987.1:c.3107G>C	XP_011534289.1:p.Ser1036Thr
XM_011535988.1:c.1970G>C	XP_011534290.1:p.Ser657Thr
NM_001346813.1:c.4829G>C	NP_001333742.1:p.Ser1610Thr
NM_001363725.1:c.2579G>C	NP_001350654.1:p.Ser860Thr
XM_011535984.2:c.5039G>C	XP_011534286.2:p.Ser1680Thr
XM_011535988.3:c.1970G>C	XP_011534290.1:p.Ser657Thr
XM_017011103.2:c.4940G>C	XP_016866592.1:p.Ser1647Thr
XM_017011104.1:c.4910G>C	XP_016866593.1:p.Ser1637Thr
XM_017011105.2:c.4880G>C	XP_016866594.1:p.Ser1627Thr
XM_017011106.2:c.4751G>C	XP_016866595.1:p.Ser1584Thr
XM_017011107.2:c.4730G>C	XP_016866596.1:p.Ser1577Thr
XR_002956289.1:n.5025G>C
NM_001363725.2:c.2579G>C	NP_001350654.1:p.Ser860Thr
NM_001371656.1:c.4958G>C	NP_001358585.1:p.Ser1653Thr
NM_001374820.1:c.4958G>C	NP_001361749.1:p.Ser1653Thr
NM_001374828.1:c.5078G>C MANE Select	NP_001361757.1:p.Ser1693Thr
NM_017519.3:c.4919G>C	NP_059989.3:p.Ser1640Thr