Canonical Allele Identifier: CA366241385

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128373835
• gnomAD v4: 6-157200990-G-A
• MyVariant Identifiers: chr6:g.157522124G>A (hg19) ; chr6:g.157200990G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200990G>A , CM000668.2:g.157200990G>A	GRCh38
NC_000006.11:g.157522124G>A , CM000668.1:g.157522124G>A	GRCh37
NC_000006.10:g.157563816G>A	NCBI36
NG_032093.1:g.428061G>A
NG_032093.2:g.428061G>A
NG_066624.1:g.429965G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4606G>A	ENSP00000055163.8:p.Ala1536Thr
ENST00000414678.8:c.4675G>A	ENSP00000412835.3:p.Ala1559Thr
ENST00000637015.2:c.4894G>A	ENSP00000489729.2:p.Ala1632Thr
ENST00000346085.10:c.4645G>A	ENSP00000344546.5:p.Ala1549Thr
ENST00000350026.10:c.4357G>A	ENSP00000055163.7:p.Ala1453Thr
ENST00000414678.7:c.2923G>A	ENSP00000412835.2:p.Ala975Thr
ENST00000635849.1:c.2086G>A	ENSP00000490948.1:p.Ala696Thr
ENST00000635957.1:c.1717G>A	ENSP00000490385.1:p.Ala573Thr
ENST00000636227.1:n.3228G>A
ENST00000636254.1:n.685G>A
ENST00000636930.2:c.4765G>A MANE Select	ENSP00000490491.2:p.Ala1589Thr
ENST00000636940.1:n.2762G>A
ENST00000637015.1:c.2133G>A
ENST00000637568.1:c.2047G>A
ENST00000637741.1:n.1431G>A
ENST00000637810.1:c.2107G>A	ENSP00000489636.1:p.Ala703Thr
ENST00000637904.1:c.2266G>A	ENSP00000490550.1:p.Ala756Thr
ENST00000647938.1:c.4396G>A	ENSP00000498155.1:p.Ala1466Thr
ENST00000346085.9:c.4396G>A	ENSP00000344546.4:p.Ala1466Thr
ENST00000350026.9:c.4357G>A	ENSP00000055163.7:p.Ala1453Thr
ENST00000414678.6:c.2923G>A	ENSP00000412835.2:p.Ala975Thr
NM_017519.2:c.4357G>A	NP_059989.2:p.Ala1453Thr
NM_020732.3:c.4396G>A	NP_065783.3:p.Ala1466Thr
XM_005267069.3:c.4516G>A	XP_005267126.2:p.Ala1506Thr
XM_011535984.1:c.3595G>A	XP_011534286.1:p.Ala1199Thr
XM_011535985.1:c.3415G>A	XP_011534287.1:p.Ala1139Thr
XM_011535986.1:c.3175G>A	XP_011534288.1:p.Ala1059Thr
XM_011535987.1:c.2794G>A	XP_011534289.1:p.Ala932Thr
XM_011535988.1:c.1657G>A	XP_011534290.1:p.Ala553Thr
NM_001346813.1:c.4516G>A	NP_001333742.1:p.Ala1506Thr
NM_001363725.1:c.2266G>A	NP_001350654.1:p.Ala756Thr
XM_011535984.2:c.4726G>A	XP_011534286.2:p.Ala1576Thr
XM_011535988.3:c.1657G>A	XP_011534290.1:p.Ala553Thr
XM_017011103.2:c.4627G>A	XP_016866592.1:p.Ala1543Thr
XM_017011104.1:c.4597G>A	XP_016866593.1:p.Ala1533Thr
XM_017011105.2:c.4567G>A	XP_016866594.1:p.Ala1523Thr
XM_017011106.2:c.4438G>A	XP_016866595.1:p.Ala1480Thr
XM_017011107.2:c.4417G>A	XP_016866596.1:p.Ala1473Thr
XR_002956289.1:n.4712G>A
NM_001363725.2:c.2266G>A	NP_001350654.1:p.Ala756Thr
NM_001371656.1:c.4645G>A	NP_001358585.1:p.Ala1549Thr
NM_001374820.1:c.4645G>A	NP_001361749.1:p.Ala1549Thr
NM_001374828.1:c.4765G>A MANE Select	NP_001361757.1:p.Ala1589Thr
NM_017519.3:c.4606G>A	NP_059989.3:p.Ala1536Thr