Canonical Allele Identifier: CA366242416

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522424C>A (hg19) ; chr6:g.157201290C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201290C>A , CM000668.2:g.157201290C>A	GRCh38
NC_000006.11:g.157522424C>A , CM000668.1:g.157522424C>A	GRCh37
NC_000006.10:g.157564116C>A	NCBI36
NG_032093.1:g.428361C>A
NG_032093.2:g.428361C>A
NG_066624.1:g.430265C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4906C>A	ENSP00000055163.8:p.Arg1636Ser
ENST00000414678.8:c.4975C>A	ENSP00000412835.3:p.Arg1659Ser
ENST00000637015.2:c.5194C>A	ENSP00000489729.2:p.Arg1732Ser
ENST00000346085.10:c.4945C>A	ENSP00000344546.5:p.Arg1649Ser
ENST00000350026.10:c.4657C>A	ENSP00000055163.7:p.Arg1553Ser
ENST00000414678.7:c.3223C>A	ENSP00000412835.2:p.Arg1075Ser
ENST00000635849.1:c.2386C>A	ENSP00000490948.1:p.Arg796Ser
ENST00000635957.1:c.2017C>A	ENSP00000490385.1:p.Arg673Ser
ENST00000636227.1:n.3528C>A
ENST00000636254.1:n.985C>A
ENST00000636930.2:c.5065C>A MANE Select	ENSP00000490491.2:p.Arg1689Ser
ENST00000636940.1:n.3062C>A
ENST00000637015.1:c.2433C>A
ENST00000637568.1:c.2347C>A
ENST00000637741.1:n.1731C>A
ENST00000637810.1:c.2407C>A	ENSP00000489636.1:p.Arg803Ser
ENST00000637904.1:c.2566C>A	ENSP00000490550.1:p.Arg856Ser
ENST00000647938.1:c.4696C>A	ENSP00000498155.1:p.Arg1566Ser
ENST00000346085.9:c.4696C>A	ENSP00000344546.4:p.Arg1566Ser
ENST00000350026.9:c.4657C>A	ENSP00000055163.7:p.Arg1553Ser
ENST00000414678.6:c.3223C>A	ENSP00000412835.2:p.Arg1075Ser
NM_017519.2:c.4657C>A	NP_059989.2:p.Arg1553Ser
NM_020732.3:c.4696C>A	NP_065783.3:p.Arg1566Ser
XM_005267069.3:c.4816C>A	XP_005267126.2:p.Arg1606Ser
XM_011535984.1:c.3895C>A	XP_011534286.1:p.Arg1299Ser
XM_011535985.1:c.3715C>A	XP_011534287.1:p.Arg1239Ser
XM_011535986.1:c.3475C>A	XP_011534288.1:p.Arg1159Ser
XM_011535987.1:c.3094C>A	XP_011534289.1:p.Arg1032Ser
XM_011535988.1:c.1957C>A	XP_011534290.1:p.Arg653Ser
NM_001346813.1:c.4816C>A	NP_001333742.1:p.Arg1606Ser
NM_001363725.1:c.2566C>A	NP_001350654.1:p.Arg856Ser
XM_011535984.2:c.5026C>A	XP_011534286.2:p.Arg1676Ser
XM_011535988.3:c.1957C>A	XP_011534290.1:p.Arg653Ser
XM_017011103.2:c.4927C>A	XP_016866592.1:p.Arg1643Ser
XM_017011104.1:c.4897C>A	XP_016866593.1:p.Arg1633Ser
XM_017011105.2:c.4867C>A	XP_016866594.1:p.Arg1623Ser
XM_017011106.2:c.4738C>A	XP_016866595.1:p.Arg1580Ser
XM_017011107.2:c.4717C>A	XP_016866596.1:p.Arg1573Ser
XR_002956289.1:n.5012C>A
NM_001363725.2:c.2566C>A	NP_001350654.1:p.Arg856Ser
NM_001371656.1:c.4945C>A	NP_001358585.1:p.Arg1649Ser
NM_001374820.1:c.4945C>A	NP_001361749.1:p.Arg1649Ser
NM_001374828.1:c.5065C>A MANE Select	NP_001361757.1:p.Arg1689Ser
NM_017519.3:c.4906C>A	NP_059989.3:p.Arg1636Ser