Canonical Allele Identifier: CA366242066

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128374768
• MyVariant Identifiers: chr6:g.157522263G>A (hg19) ; chr6:g.157201129G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201129G>A , CM000668.2:g.157201129G>A	GRCh38
NC_000006.11:g.157522263G>A , CM000668.1:g.157522263G>A	GRCh37
NC_000006.10:g.157563955G>A	NCBI36
NG_032093.1:g.428200G>A
NG_032093.2:g.428200G>A
NG_066624.1:g.430104G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4745G>A	ENSP00000055163.8:p.Trp1582Ter
ENST00000414678.8:c.4814G>A	ENSP00000412835.3:p.Trp1605Ter
ENST00000637015.2:c.5033G>A	ENSP00000489729.2:p.Trp1678Ter
ENST00000346085.10:c.4784G>A	ENSP00000344546.5:p.Trp1595Ter
ENST00000350026.10:c.4496G>A	ENSP00000055163.7:p.Trp1499Ter
ENST00000414678.7:c.3062G>A	ENSP00000412835.2:p.Trp1021Ter
ENST00000635849.1:c.2225G>A	ENSP00000490948.1:p.Trp742Ter
ENST00000635957.1:c.1856G>A	ENSP00000490385.1:p.Trp619Ter
ENST00000636227.1:n.3367G>A
ENST00000636254.1:n.824G>A
ENST00000636930.2:c.4904G>A MANE Select	ENSP00000490491.2:p.Trp1635Ter
ENST00000636940.1:n.2901G>A
ENST00000637015.1:c.2272G>A
ENST00000637568.1:c.2186G>A
ENST00000637741.1:n.1570G>A
ENST00000637810.1:c.2246G>A	ENSP00000489636.1:p.Trp749Ter
ENST00000637904.1:c.2405G>A	ENSP00000490550.1:p.Trp802Ter
ENST00000647938.1:c.4535G>A	ENSP00000498155.1:p.Trp1512Ter
ENST00000346085.9:c.4535G>A	ENSP00000344546.4:p.Trp1512Ter
ENST00000350026.9:c.4496G>A	ENSP00000055163.7:p.Trp1499Ter
ENST00000414678.6:c.3062G>A	ENSP00000412835.2:p.Trp1021Ter
NM_017519.2:c.4496G>A	NP_059989.2:p.Trp1499Ter
NM_020732.3:c.4535G>A	NP_065783.3:p.Trp1512Ter
XM_005267069.3:c.4655G>A	XP_005267126.2:p.Trp1552Ter
XM_011535984.1:c.3734G>A	XP_011534286.1:p.Trp1245Ter
XM_011535985.1:c.3554G>A	XP_011534287.1:p.Trp1185Ter
XM_011535986.1:c.3314G>A	XP_011534288.1:p.Trp1105Ter
XM_011535987.1:c.2933G>A	XP_011534289.1:p.Trp978Ter
XM_011535988.1:c.1796G>A	XP_011534290.1:p.Trp599Ter
NM_001346813.1:c.4655G>A	NP_001333742.1:p.Trp1552Ter
NM_001363725.1:c.2405G>A	NP_001350654.1:p.Trp802Ter
XM_011535984.2:c.4865G>A	XP_011534286.2:p.Trp1622Ter
XM_011535988.3:c.1796G>A	XP_011534290.1:p.Trp599Ter
XM_017011103.2:c.4766G>A	XP_016866592.1:p.Trp1589Ter
XM_017011104.1:c.4736G>A	XP_016866593.1:p.Trp1579Ter
XM_017011105.2:c.4706G>A	XP_016866594.1:p.Trp1569Ter
XM_017011106.2:c.4577G>A	XP_016866595.1:p.Trp1526Ter
XM_017011107.2:c.4556G>A	XP_016866596.1:p.Trp1519Ter
XR_002956289.1:n.4851G>A
NM_001363725.2:c.2405G>A	NP_001350654.1:p.Trp802Ter
NM_001371656.1:c.4784G>A	NP_001358585.1:p.Trp1595Ter
NM_001374820.1:c.4784G>A	NP_001361749.1:p.Trp1595Ter
NM_001374828.1:c.4904G>A MANE Select	NP_001361757.1:p.Trp1635Ter
NM_017519.3:c.4745G>A	NP_059989.3:p.Trp1582Ter