Canonical Allele Identifier: CA366241152

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128373180
• gnomAD v4: 6-157200886-G-A
• MyVariant Identifiers: chr6:g.157522020G>A (hg19) ; chr6:g.157200886G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200886G>A , CM000668.2:g.157200886G>A	GRCh38
NC_000006.11:g.157522020G>A , CM000668.1:g.157522020G>A	GRCh37
NC_000006.10:g.157563712G>A	NCBI36
NG_032093.1:g.427957G>A
NG_032093.2:g.427957G>A
NG_066624.1:g.429861G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4502G>A	ENSP00000055163.8:p.Arg1501Lys
ENST00000414678.8:c.4571G>A	ENSP00000412835.3:p.Arg1524Lys
ENST00000637015.2:c.4790G>A	ENSP00000489729.2:p.Arg1597Lys
ENST00000346085.10:c.4541G>A	ENSP00000344546.5:p.Arg1514Lys
ENST00000350026.10:c.4253G>A	ENSP00000055163.7:p.Arg1418Lys
ENST00000414678.7:c.2819G>A	ENSP00000412835.2:p.Arg940Lys
ENST00000635849.1:c.1982G>A	ENSP00000490948.1:p.Arg661Lys
ENST00000635957.1:c.1613G>A	ENSP00000490385.1:p.Arg538Lys
ENST00000636227.1:n.3124G>A
ENST00000636254.1:n.581G>A
ENST00000636930.2:c.4661G>A MANE Select	ENSP00000490491.2:p.Arg1554Lys
ENST00000636940.1:n.2658G>A
ENST00000637015.1:c.2029G>A
ENST00000637568.1:c.1943G>A
ENST00000637741.1:n.1327G>A
ENST00000637810.1:c.2003G>A	ENSP00000489636.1:p.Arg668Lys
ENST00000637904.1:c.2162G>A	ENSP00000490550.1:p.Arg721Lys
ENST00000647938.1:c.4292G>A	ENSP00000498155.1:p.Arg1431Lys
ENST00000346085.9:c.4292G>A	ENSP00000344546.4:p.Arg1431Lys
ENST00000350026.9:c.4253G>A	ENSP00000055163.7:p.Arg1418Lys
ENST00000414678.6:c.2819G>A	ENSP00000412835.2:p.Arg940Lys
NM_017519.2:c.4253G>A	NP_059989.2:p.Arg1418Lys
NM_020732.3:c.4292G>A	NP_065783.3:p.Arg1431Lys
XM_005267069.3:c.4412G>A	XP_005267126.2:p.Arg1471Lys
XM_011535984.1:c.3491G>A	XP_011534286.1:p.Arg1164Lys
XM_011535985.1:c.3311G>A	XP_011534287.1:p.Arg1104Lys
XM_011535986.1:c.3071G>A	XP_011534288.1:p.Arg1024Lys
XM_011535987.1:c.2690G>A	XP_011534289.1:p.Arg897Lys
XM_011535988.1:c.1553G>A	XP_011534290.1:p.Arg518Lys
NM_001346813.1:c.4412G>A	NP_001333742.1:p.Arg1471Lys
NM_001363725.1:c.2162G>A	NP_001350654.1:p.Arg721Lys
XM_011535984.2:c.4622G>A	XP_011534286.2:p.Arg1541Lys
XM_011535988.3:c.1553G>A	XP_011534290.1:p.Arg518Lys
XM_017011103.2:c.4523G>A	XP_016866592.1:p.Arg1508Lys
XM_017011104.1:c.4493G>A	XP_016866593.1:p.Arg1498Lys
XM_017011105.2:c.4463G>A	XP_016866594.1:p.Arg1488Lys
XM_017011106.2:c.4334G>A	XP_016866595.1:p.Arg1445Lys
XM_017011107.2:c.4313G>A	XP_016866596.1:p.Arg1438Lys
XR_002956289.1:n.4608G>A
NM_001363725.2:c.2162G>A	NP_001350654.1:p.Arg721Lys
NM_001371656.1:c.4541G>A	NP_001358585.1:p.Arg1514Lys
NM_001374820.1:c.4541G>A	NP_001361749.1:p.Arg1514Lys
NM_001374828.1:c.4661G>A MANE Select	NP_001361757.1:p.Arg1554Lys
NM_017519.3:c.4502G>A	NP_059989.3:p.Arg1501Lys