Canonical Allele Identifier: CA366242261

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522350A>C (hg19) ; chr6:g.157201216A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201216A>C , CM000668.2:g.157201216A>C	GRCh38
NC_000006.11:g.157522350A>C , CM000668.1:g.157522350A>C	GRCh37
NC_000006.10:g.157564042A>C	NCBI36
NG_032093.1:g.428287A>C
NG_032093.2:g.428287A>C
NG_066624.1:g.430191A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4832A>C	ENSP00000055163.8:p.Gln1611Pro
ENST00000414678.8:c.4901A>C	ENSP00000412835.3:p.Gln1634Pro
ENST00000637015.2:c.5120A>C	ENSP00000489729.2:p.Gln1707Pro
ENST00000346085.10:c.4871A>C	ENSP00000344546.5:p.Gln1624Pro
ENST00000350026.10:c.4583A>C	ENSP00000055163.7:p.Gln1528Pro
ENST00000414678.7:c.3149A>C	ENSP00000412835.2:p.Gln1050Pro
ENST00000635849.1:c.2312A>C	ENSP00000490948.1:p.Gln771Pro
ENST00000635957.1:c.1943A>C	ENSP00000490385.1:p.Gln648Pro
ENST00000636227.1:n.3454A>C
ENST00000636254.1:n.911A>C
ENST00000636930.2:c.4991A>C MANE Select	ENSP00000490491.2:p.Gln1664Pro
ENST00000636940.1:n.2988A>C
ENST00000637015.1:c.2359A>C
ENST00000637568.1:c.2273A>C
ENST00000637741.1:n.1657A>C
ENST00000637810.1:c.2333A>C	ENSP00000489636.1:p.Gln778Pro
ENST00000637904.1:c.2492A>C	ENSP00000490550.1:p.Gln831Pro
ENST00000647938.1:c.4622A>C	ENSP00000498155.1:p.Gln1541Pro
ENST00000346085.9:c.4622A>C	ENSP00000344546.4:p.Gln1541Pro
ENST00000350026.9:c.4583A>C	ENSP00000055163.7:p.Gln1528Pro
ENST00000414678.6:c.3149A>C	ENSP00000412835.2:p.Gln1050Pro
NM_017519.2:c.4583A>C	NP_059989.2:p.Gln1528Pro
NM_020732.3:c.4622A>C	NP_065783.3:p.Gln1541Pro
XM_005267069.3:c.4742A>C	XP_005267126.2:p.Gln1581Pro
XM_011535984.1:c.3821A>C	XP_011534286.1:p.Gln1274Pro
XM_011535985.1:c.3641A>C	XP_011534287.1:p.Gln1214Pro
XM_011535986.1:c.3401A>C	XP_011534288.1:p.Gln1134Pro
XM_011535987.1:c.3020A>C	XP_011534289.1:p.Gln1007Pro
XM_011535988.1:c.1883A>C	XP_011534290.1:p.Gln628Pro
NM_001346813.1:c.4742A>C	NP_001333742.1:p.Gln1581Pro
NM_001363725.1:c.2492A>C	NP_001350654.1:p.Gln831Pro
XM_011535984.2:c.4952A>C	XP_011534286.2:p.Gln1651Pro
XM_011535988.3:c.1883A>C	XP_011534290.1:p.Gln628Pro
XM_017011103.2:c.4853A>C	XP_016866592.1:p.Gln1618Pro
XM_017011104.1:c.4823A>C	XP_016866593.1:p.Gln1608Pro
XM_017011105.2:c.4793A>C	XP_016866594.1:p.Gln1598Pro
XM_017011106.2:c.4664A>C	XP_016866595.1:p.Gln1555Pro
XM_017011107.2:c.4643A>C	XP_016866596.1:p.Gln1548Pro
XR_002956289.1:n.4938A>C
NM_001363725.2:c.2492A>C	NP_001350654.1:p.Gln831Pro
NM_001371656.1:c.4871A>C	NP_001358585.1:p.Gln1624Pro
NM_001374820.1:c.4871A>C	NP_001361749.1:p.Gln1624Pro
NM_001374828.1:c.4991A>C MANE Select	NP_001361757.1:p.Gln1664Pro
NM_017519.3:c.4832A>C	NP_059989.3:p.Gln1611Pro