Canonical Allele Identifier: CA366242549

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522461T>G (hg19) ; chr6:g.157201327T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201327T>G , CM000668.2:g.157201327T>G	GRCh38
NC_000006.11:g.157522461T>G , CM000668.1:g.157522461T>G	GRCh37
NC_000006.10:g.157564153T>G	NCBI36
NG_032093.1:g.428398T>G
NG_032093.2:g.428398T>G
NG_066624.1:g.430302T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4943T>G	ENSP00000055163.8:p.Met1648Arg
ENST00000414678.8:c.5012T>G	ENSP00000412835.3:p.Met1671Arg
ENST00000637015.2:c.5231T>G	ENSP00000489729.2:p.Met1744Arg
ENST00000346085.10:c.4982T>G	ENSP00000344546.5:p.Met1661Arg
ENST00000350026.10:c.4694T>G	ENSP00000055163.7:p.Met1565Arg
ENST00000414678.7:c.3260T>G	ENSP00000412835.2:p.Met1087Arg
ENST00000635849.1:c.2423T>G	ENSP00000490948.1:p.Met808Arg
ENST00000635957.1:c.2054T>G	ENSP00000490385.1:p.Met685Arg
ENST00000636227.1:n.3565T>G
ENST00000636254.1:n.1022T>G
ENST00000636930.2:c.5102T>G MANE Select	ENSP00000490491.2:p.Met1701Arg
ENST00000636940.1:n.3099T>G
ENST00000637015.1:c.2470T>G
ENST00000637568.1:c.2384T>G
ENST00000637741.1:n.1768T>G
ENST00000637810.1:c.2444T>G	ENSP00000489636.1:p.Met815Arg
ENST00000637904.1:c.2603T>G	ENSP00000490550.1:p.Met868Arg
ENST00000647938.1:c.4733T>G	ENSP00000498155.1:p.Met1578Arg
ENST00000346085.9:c.4733T>G	ENSP00000344546.4:p.Met1578Arg
ENST00000350026.9:c.4694T>G	ENSP00000055163.7:p.Met1565Arg
ENST00000414678.6:c.3260T>G	ENSP00000412835.2:p.Met1087Arg
NM_017519.2:c.4694T>G	NP_059989.2:p.Met1565Arg
NM_020732.3:c.4733T>G	NP_065783.3:p.Met1578Arg
XM_005267069.3:c.4853T>G	XP_005267126.2:p.Met1618Arg
XM_011535984.1:c.3932T>G	XP_011534286.1:p.Met1311Arg
XM_011535985.1:c.3752T>G	XP_011534287.1:p.Met1251Arg
XM_011535986.1:c.3512T>G	XP_011534288.1:p.Met1171Arg
XM_011535987.1:c.3131T>G	XP_011534289.1:p.Met1044Arg
XM_011535988.1:c.1994T>G	XP_011534290.1:p.Met665Arg
NM_001346813.1:c.4853T>G	NP_001333742.1:p.Met1618Arg
NM_001363725.1:c.2603T>G	NP_001350654.1:p.Met868Arg
XM_011535984.2:c.5063T>G	XP_011534286.2:p.Met1688Arg
XM_011535988.3:c.1994T>G	XP_011534290.1:p.Met665Arg
XM_017011103.2:c.4964T>G	XP_016866592.1:p.Met1655Arg
XM_017011104.1:c.4934T>G	XP_016866593.1:p.Met1645Arg
XM_017011105.2:c.4904T>G	XP_016866594.1:p.Met1635Arg
XM_017011106.2:c.4775T>G	XP_016866595.1:p.Met1592Arg
XM_017011107.2:c.4754T>G	XP_016866596.1:p.Met1585Arg
XR_002956289.1:n.5049T>G
NM_001363725.2:c.2603T>G	NP_001350654.1:p.Met868Arg
NM_001371656.1:c.4982T>G	NP_001358585.1:p.Met1661Arg
NM_001374820.1:c.4982T>G	NP_001361749.1:p.Met1661Arg
NM_001374828.1:c.5102T>G MANE Select	NP_001361757.1:p.Met1701Arg
NM_017519.3:c.4943T>G	NP_059989.3:p.Met1648Arg