Canonical Allele Identifier: CA366241156

Gene: ARID1B

Linked Data

• ClinVar Variation Id: 2627084
• ClinVar RCV Id: RCV003388282
• MyVariant Identifiers: chr6:g.157522021G>T (hg19) ; chr6:g.157200887G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200887G>T , CM000668.2:g.157200887G>T	GRCh38
NC_000006.11:g.157522021G>T , CM000668.1:g.157522021G>T	GRCh37
NC_000006.10:g.157563713G>T	NCBI36
NG_032093.1:g.427958G>T
NG_032093.2:g.427958G>T
NG_066624.1:g.429862G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4503G>T	ENSP00000055163.8:p.Arg1501Ser
ENST00000414678.8:c.4572G>T	ENSP00000412835.3:p.Arg1524Ser
ENST00000637015.2:c.4791G>T	ENSP00000489729.2:p.Arg1597Ser
ENST00000346085.10:c.4542G>T	ENSP00000344546.5:p.Arg1514Ser
ENST00000350026.10:c.4254G>T	ENSP00000055163.7:p.Arg1418Ser
ENST00000414678.7:c.2820G>T	ENSP00000412835.2:p.Arg940Ser
ENST00000635849.1:c.1983G>T	ENSP00000490948.1:p.Arg661Ser
ENST00000635957.1:c.1614G>T	ENSP00000490385.1:p.Arg538Ser
ENST00000636227.1:n.3125G>T
ENST00000636254.1:n.582G>T
ENST00000636930.2:c.4662G>T MANE Select	ENSP00000490491.2:p.Arg1554Ser
ENST00000636940.1:n.2659G>T
ENST00000637015.1:c.2030G>T
ENST00000637568.1:c.1944G>T
ENST00000637741.1:n.1328G>T
ENST00000637810.1:c.2004G>T	ENSP00000489636.1:p.Arg668Ser
ENST00000637904.1:c.2163G>T	ENSP00000490550.1:p.Arg721Ser
ENST00000647938.1:c.4293G>T	ENSP00000498155.1:p.Arg1431Ser
ENST00000346085.9:c.4293G>T	ENSP00000344546.4:p.Arg1431Ser
ENST00000350026.9:c.4254G>T	ENSP00000055163.7:p.Arg1418Ser
ENST00000414678.6:c.2820G>T	ENSP00000412835.2:p.Arg940Ser
NM_017519.2:c.4254G>T	NP_059989.2:p.Arg1418Ser
NM_020732.3:c.4293G>T	NP_065783.3:p.Arg1431Ser
XM_005267069.3:c.4413G>T	XP_005267126.2:p.Arg1471Ser
XM_011535984.1:c.3492G>T	XP_011534286.1:p.Arg1164Ser
XM_011535985.1:c.3312G>T	XP_011534287.1:p.Arg1104Ser
XM_011535986.1:c.3072G>T	XP_011534288.1:p.Arg1024Ser
XM_011535987.1:c.2691G>T	XP_011534289.1:p.Arg897Ser
XM_011535988.1:c.1554G>T	XP_011534290.1:p.Arg518Ser
NM_001346813.1:c.4413G>T	NP_001333742.1:p.Arg1471Ser
NM_001363725.1:c.2163G>T	NP_001350654.1:p.Arg721Ser
XM_011535984.2:c.4623G>T	XP_011534286.2:p.Arg1541Ser
XM_011535988.3:c.1554G>T	XP_011534290.1:p.Arg518Ser
XM_017011103.2:c.4524G>T	XP_016866592.1:p.Arg1508Ser
XM_017011104.1:c.4494G>T	XP_016866593.1:p.Arg1498Ser
XM_017011105.2:c.4464G>T	XP_016866594.1:p.Arg1488Ser
XM_017011106.2:c.4335G>T	XP_016866595.1:p.Arg1445Ser
XM_017011107.2:c.4314G>T	XP_016866596.1:p.Arg1438Ser
XR_002956289.1:n.4609G>T
NM_001363725.2:c.2163G>T	NP_001350654.1:p.Arg721Ser
NM_001371656.1:c.4542G>T	NP_001358585.1:p.Arg1514Ser
NM_001374820.1:c.4542G>T	NP_001361749.1:p.Arg1514Ser
NM_001374828.1:c.4662G>T MANE Select	NP_001361757.1:p.Arg1554Ser
NM_017519.3:c.4503G>T	NP_059989.3:p.Arg1501Ser