Canonical Allele Identifier: CA366241386

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522124G>T (hg19) ; chr6:g.157200990G>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4606G>T	ENSP00000055163.8:p.Ala1536Ser
ENST00000414678.8:c.4675G>T	ENSP00000412835.3:p.Ala1559Ser
ENST00000637015.2:c.4894G>T	ENSP00000489729.2:p.Ala1632Ser
ENST00000346085.10:c.4645G>T	ENSP00000344546.5:p.Ala1549Ser
ENST00000350026.10:c.4357G>T	ENSP00000055163.7:p.Ala1453Ser
ENST00000414678.7:c.2923G>T	ENSP00000412835.2:p.Ala975Ser
ENST00000635849.1:c.2086G>T	ENSP00000490948.1:p.Ala696Ser
ENST00000635957.1:c.1717G>T	ENSP00000490385.1:p.Ala573Ser
ENST00000636227.1:n.3228G>T
ENST00000636254.1:n.685G>T
ENST00000636930.2:c.4765G>T MANE Select	ENSP00000490491.2:p.Ala1589Ser
ENST00000636940.1:n.2762G>T
ENST00000637015.1:c.2133G>T
ENST00000637568.1:c.2047G>T
ENST00000637741.1:n.1431G>T
ENST00000637810.1:c.2107G>T	ENSP00000489636.1:p.Ala703Ser
ENST00000637904.1:c.2266G>T	ENSP00000490550.1:p.Ala756Ser
ENST00000647938.1:c.4396G>T	ENSP00000498155.1:p.Ala1466Ser
ENST00000346085.9:c.4396G>T	ENSP00000344546.4:p.Ala1466Ser
ENST00000350026.9:c.4357G>T	ENSP00000055163.7:p.Ala1453Ser
ENST00000414678.6:c.2923G>T	ENSP00000412835.2:p.Ala975Ser
NM_017519.2:c.4357G>T	NP_059989.2:p.Ala1453Ser
NM_020732.3:c.4396G>T	NP_065783.3:p.Ala1466Ser
XM_005267069.3:c.4516G>T	XP_005267126.2:p.Ala1506Ser
XM_011535984.1:c.3595G>T	XP_011534286.1:p.Ala1199Ser
XM_011535985.1:c.3415G>T	XP_011534287.1:p.Ala1139Ser
XM_011535986.1:c.3175G>T	XP_011534288.1:p.Ala1059Ser
XM_011535987.1:c.2794G>T	XP_011534289.1:p.Ala932Ser
XM_011535988.1:c.1657G>T	XP_011534290.1:p.Ala553Ser
NM_001346813.1:c.4516G>T	NP_001333742.1:p.Ala1506Ser
NM_001363725.1:c.2266G>T	NP_001350654.1:p.Ala756Ser
XM_011535984.2:c.4726G>T	XP_011534286.2:p.Ala1576Ser
XM_011535988.3:c.1657G>T	XP_011534290.1:p.Ala553Ser
XM_017011103.2:c.4627G>T	XP_016866592.1:p.Ala1543Ser
XM_017011104.1:c.4597G>T	XP_016866593.1:p.Ala1533Ser
XM_017011105.2:c.4567G>T	XP_016866594.1:p.Ala1523Ser
XM_017011106.2:c.4438G>T	XP_016866595.1:p.Ala1480Ser
XM_017011107.2:c.4417G>T	XP_016866596.1:p.Ala1473Ser
XR_002956289.1:n.4712G>T
NM_001363725.2:c.2266G>T	NP_001350654.1:p.Ala756Ser
NM_001371656.1:c.4645G>T	NP_001358585.1:p.Ala1549Ser
NM_001374820.1:c.4645G>T	NP_001361749.1:p.Ala1549Ser
NM_001374828.1:c.4765G>T MANE Select	NP_001361757.1:p.Ala1589Ser
NM_017519.3:c.4606G>T	NP_059989.3:p.Ala1536Ser