Canonical Allele Identifier: CA366242758

Gene: ARID1B

Linked Data

• dbSNP Id: rs1554235971
• MyVariant Identifiers: chr6:g.157522499C>A (hg19) ; chr6:g.157201365C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201365C>A , CM000668.2:g.157201365C>A	GRCh38
NC_000006.11:g.157522499C>A , CM000668.1:g.157522499C>A	GRCh37
NC_000006.10:g.157564191C>A	NCBI36
NG_032093.1:g.428436C>A
NG_032093.2:g.428436C>A
NG_066624.1:g.430340C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4981C>A	ENSP00000055163.8:p.Gln1661Lys
ENST00000414678.8:c.5050C>A	ENSP00000412835.3:p.Gln1684Lys
ENST00000637015.2:c.5269C>A	ENSP00000489729.2:p.Gln1757Lys
ENST00000346085.10:c.5020C>A	ENSP00000344546.5:p.Gln1674Lys
ENST00000350026.10:c.4732C>A	ENSP00000055163.7:p.Gln1578Lys
ENST00000414678.7:c.3298C>A	ENSP00000412835.2:p.Gln1100Lys
ENST00000635849.1:c.2461C>A	ENSP00000490948.1:p.Gln821Lys
ENST00000635957.1:c.2092C>A	ENSP00000490385.1:p.Gln698Lys
ENST00000636227.1:n.3603C>A
ENST00000636254.1:n.1060C>A
ENST00000636930.2:c.5140C>A MANE Select	ENSP00000490491.2:p.Gln1714Lys
ENST00000636940.1:n.3137C>A
ENST00000637015.1:c.2508C>A
ENST00000637568.1:c.2422C>A
ENST00000637741.1:n.1806C>A
ENST00000637810.1:c.2482C>A	ENSP00000489636.1:p.Gln828Lys
ENST00000637904.1:c.2641C>A	ENSP00000490550.1:p.Gln881Lys
ENST00000647938.1:c.4771C>A	ENSP00000498155.1:p.Gln1591Lys
ENST00000346085.9:c.4771C>A	ENSP00000344546.4:p.Gln1591Lys
ENST00000350026.9:c.4732C>A	ENSP00000055163.7:p.Gln1578Lys
ENST00000414678.6:c.3298C>A	ENSP00000412835.2:p.Gln1100Lys
NM_017519.2:c.4732C>A	NP_059989.2:p.Gln1578Lys
NM_020732.3:c.4771C>A	NP_065783.3:p.Gln1591Lys
XM_005267069.3:c.4891C>A	XP_005267126.2:p.Gln1631Lys
XM_011535984.1:c.3970C>A	XP_011534286.1:p.Gln1324Lys
XM_011535985.1:c.3790C>A	XP_011534287.1:p.Gln1264Lys
XM_011535986.1:c.3550C>A	XP_011534288.1:p.Gln1184Lys
XM_011535987.1:c.3169C>A	XP_011534289.1:p.Gln1057Lys
XM_011535988.1:c.2032C>A	XP_011534290.1:p.Gln678Lys
NM_001346813.1:c.4891C>A	NP_001333742.1:p.Gln1631Lys
NM_001363725.1:c.2641C>A	NP_001350654.1:p.Gln881Lys
XM_011535984.2:c.5101C>A	XP_011534286.2:p.Gln1701Lys
XM_011535988.3:c.2032C>A	XP_011534290.1:p.Gln678Lys
XM_017011103.2:c.5002C>A	XP_016866592.1:p.Gln1668Lys
XM_017011104.1:c.4972C>A	XP_016866593.1:p.Gln1658Lys
XM_017011105.2:c.4942C>A	XP_016866594.1:p.Gln1648Lys
XM_017011106.2:c.4813C>A	XP_016866595.1:p.Gln1605Lys
XM_017011107.2:c.4792C>A	XP_016866596.1:p.Gln1598Lys
XR_002956289.1:n.5087C>A
NM_001363725.2:c.2641C>A	NP_001350654.1:p.Gln881Lys
NM_001371656.1:c.5020C>A	NP_001358585.1:p.Gln1674Lys
NM_001374820.1:c.5020C>A	NP_001361749.1:p.Gln1674Lys
NM_001374828.1:c.5140C>A MANE Select	NP_001361757.1:p.Gln1714Lys
NM_017519.3:c.4981C>A	NP_059989.3:p.Gln1661Lys