Canonical Allele Identifier: CA366242401

Gene: ARID1B

Linked Data

• dbSNP Id: rs1554235925
• MyVariant Identifiers: chr6:g.157522418G>T (hg19) ; chr6:g.157201284G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201284G>T , CM000668.2:g.157201284G>T	GRCh38
NC_000006.11:g.157522418G>T , CM000668.1:g.157522418G>T	GRCh37
NC_000006.10:g.157564110G>T	NCBI36
NG_032093.1:g.428355G>T
NG_032093.2:g.428355G>T
NG_066624.1:g.430259G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4900G>T	ENSP00000055163.8:p.Glu1634Ter
ENST00000414678.8:c.4969G>T	ENSP00000412835.3:p.Glu1657Ter
ENST00000637015.2:c.5188G>T	ENSP00000489729.2:p.Glu1730Ter
ENST00000346085.10:c.4939G>T	ENSP00000344546.5:p.Glu1647Ter
ENST00000350026.10:c.4651G>T	ENSP00000055163.7:p.Glu1551Ter
ENST00000414678.7:c.3217G>T	ENSP00000412835.2:p.Glu1073Ter
ENST00000635849.1:c.2380G>T	ENSP00000490948.1:p.Glu794Ter
ENST00000635957.1:c.2011G>T	ENSP00000490385.1:p.Glu671Ter
ENST00000636227.1:n.3522G>T
ENST00000636254.1:n.979G>T
ENST00000636930.2:c.5059G>T MANE Select	ENSP00000490491.2:p.Glu1687Ter
ENST00000636940.1:n.3056G>T
ENST00000637015.1:c.2427G>T
ENST00000637568.1:c.2341G>T
ENST00000637741.1:n.1725G>T
ENST00000637810.1:c.2401G>T	ENSP00000489636.1:p.Glu801Ter
ENST00000637904.1:c.2560G>T	ENSP00000490550.1:p.Glu854Ter
ENST00000647938.1:c.4690G>T	ENSP00000498155.1:p.Glu1564Ter
ENST00000346085.9:c.4690G>T	ENSP00000344546.4:p.Glu1564Ter
ENST00000350026.9:c.4651G>T	ENSP00000055163.7:p.Glu1551Ter
ENST00000414678.6:c.3217G>T	ENSP00000412835.2:p.Glu1073Ter
NM_017519.2:c.4651G>T	NP_059989.2:p.Glu1551Ter
NM_020732.3:c.4690G>T	NP_065783.3:p.Glu1564Ter
XM_005267069.3:c.4810G>T	XP_005267126.2:p.Glu1604Ter
XM_011535984.1:c.3889G>T	XP_011534286.1:p.Glu1297Ter
XM_011535985.1:c.3709G>T	XP_011534287.1:p.Glu1237Ter
XM_011535986.1:c.3469G>T	XP_011534288.1:p.Glu1157Ter
XM_011535987.1:c.3088G>T	XP_011534289.1:p.Glu1030Ter
XM_011535988.1:c.1951G>T	XP_011534290.1:p.Glu651Ter
NM_001346813.1:c.4810G>T	NP_001333742.1:p.Glu1604Ter
NM_001363725.1:c.2560G>T	NP_001350654.1:p.Glu854Ter
XM_011535984.2:c.5020G>T	XP_011534286.2:p.Glu1674Ter
XM_011535988.3:c.1951G>T	XP_011534290.1:p.Glu651Ter
XM_017011103.2:c.4921G>T	XP_016866592.1:p.Glu1641Ter
XM_017011104.1:c.4891G>T	XP_016866593.1:p.Glu1631Ter
XM_017011105.2:c.4861G>T	XP_016866594.1:p.Glu1621Ter
XM_017011106.2:c.4732G>T	XP_016866595.1:p.Glu1578Ter
XM_017011107.2:c.4711G>T	XP_016866596.1:p.Glu1571Ter
XR_002956289.1:n.5006G>T
NM_001363725.2:c.2560G>T	NP_001350654.1:p.Glu854Ter
NM_001371656.1:c.4939G>T	NP_001358585.1:p.Glu1647Ter
NM_001374820.1:c.4939G>T	NP_001361749.1:p.Glu1647Ter
NM_001374828.1:c.5059G>T MANE Select	NP_001361757.1:p.Glu1687Ter
NM_017519.3:c.4900G>T	NP_059989.3:p.Glu1634Ter