Canonical Allele Identifier: CA366242836

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522515C>A (hg19) ; chr6:g.157201381C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201381C>A , CM000668.2:g.157201381C>A	GRCh38
NC_000006.11:g.157522515C>A , CM000668.1:g.157522515C>A	GRCh37
NC_000006.10:g.157564207C>A	NCBI36
NG_032093.1:g.428452C>A
NG_032093.2:g.428452C>A
NG_066624.1:g.430356C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4997C>A	ENSP00000055163.8:p.Pro1666Gln
ENST00000414678.8:c.5066C>A	ENSP00000412835.3:p.Pro1689Gln
ENST00000637015.2:c.5285C>A	ENSP00000489729.2:p.Pro1762Gln
ENST00000346085.10:c.5036C>A	ENSP00000344546.5:p.Pro1679Gln
ENST00000350026.10:c.4748C>A	ENSP00000055163.7:p.Pro1583Gln
ENST00000414678.7:c.3314C>A	ENSP00000412835.2:p.Pro1105Gln
ENST00000635849.1:c.2477C>A	ENSP00000490948.1:p.Pro826Gln
ENST00000635957.1:c.2108C>A	ENSP00000490385.1:p.Pro703Gln
ENST00000636227.1:n.3619C>A
ENST00000636254.1:n.1076C>A
ENST00000636930.2:c.5156C>A MANE Select	ENSP00000490491.2:p.Pro1719Gln
ENST00000636940.1:n.3153C>A
ENST00000637015.1:c.2524C>A
ENST00000637568.1:c.2438C>A
ENST00000637741.1:n.1822C>A
ENST00000637810.1:c.2498C>A	ENSP00000489636.1:p.Pro833Gln
ENST00000637904.1:c.2657C>A	ENSP00000490550.1:p.Pro886Gln
ENST00000647938.1:c.4787C>A	ENSP00000498155.1:p.Pro1596Gln
ENST00000346085.9:c.4787C>A	ENSP00000344546.4:p.Pro1596Gln
ENST00000350026.9:c.4748C>A	ENSP00000055163.7:p.Pro1583Gln
ENST00000414678.6:c.3314C>A	ENSP00000412835.2:p.Pro1105Gln
NM_017519.2:c.4748C>A	NP_059989.2:p.Pro1583Gln
NM_020732.3:c.4787C>A	NP_065783.3:p.Pro1596Gln
XM_005267069.3:c.4907C>A	XP_005267126.2:p.Pro1636Gln
XM_011535984.1:c.3986C>A	XP_011534286.1:p.Pro1329Gln
XM_011535985.1:c.3806C>A	XP_011534287.1:p.Pro1269Gln
XM_011535986.1:c.3566C>A	XP_011534288.1:p.Pro1189Gln
XM_011535987.1:c.3185C>A	XP_011534289.1:p.Pro1062Gln
XM_011535988.1:c.2048C>A	XP_011534290.1:p.Pro683Gln
NM_001346813.1:c.4907C>A	NP_001333742.1:p.Pro1636Gln
NM_001363725.1:c.2657C>A	NP_001350654.1:p.Pro886Gln
XM_011535984.2:c.5117C>A	XP_011534286.2:p.Pro1706Gln
XM_011535988.3:c.2048C>A	XP_011534290.1:p.Pro683Gln
XM_017011103.2:c.5018C>A	XP_016866592.1:p.Pro1673Gln
XM_017011104.1:c.4988C>A	XP_016866593.1:p.Pro1663Gln
XM_017011105.2:c.4958C>A	XP_016866594.1:p.Pro1653Gln
XM_017011106.2:c.4829C>A	XP_016866595.1:p.Pro1610Gln
XM_017011107.2:c.4808C>A	XP_016866596.1:p.Pro1603Gln
XR_002956289.1:n.5103C>A
NM_001363725.2:c.2657C>A	NP_001350654.1:p.Pro886Gln
NM_001371656.1:c.5036C>A	NP_001358585.1:p.Pro1679Gln
NM_001374820.1:c.5036C>A	NP_001361749.1:p.Pro1679Gln
NM_001374828.1:c.5156C>A MANE Select	NP_001361757.1:p.Pro1719Gln
NM_017519.3:c.4997C>A	NP_059989.3:p.Pro1666Gln