Canonical Allele Identifier: CA366242611

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522470A>T (hg19) ; chr6:g.157201336A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201336A>T , CM000668.2:g.157201336A>T	GRCh38
NC_000006.11:g.157522470A>T , CM000668.1:g.157522470A>T	GRCh37
NC_000006.10:g.157564162A>T	NCBI36
NG_032093.1:g.428407A>T
NG_032093.2:g.428407A>T
NG_066624.1:g.430311A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4952A>T	ENSP00000055163.8:p.Gln1651Leu
ENST00000414678.8:c.5021A>T	ENSP00000412835.3:p.Gln1674Leu
ENST00000637015.2:c.5240A>T	ENSP00000489729.2:p.Gln1747Leu
ENST00000346085.10:c.4991A>T	ENSP00000344546.5:p.Gln1664Leu
ENST00000350026.10:c.4703A>T	ENSP00000055163.7:p.Gln1568Leu
ENST00000414678.7:c.3269A>T	ENSP00000412835.2:p.Gln1090Leu
ENST00000635849.1:c.2432A>T	ENSP00000490948.1:p.Gln811Leu
ENST00000635957.1:c.2063A>T	ENSP00000490385.1:p.Gln688Leu
ENST00000636227.1:n.3574A>T
ENST00000636254.1:n.1031A>T
ENST00000636930.2:c.5111A>T MANE Select	ENSP00000490491.2:p.Gln1704Leu
ENST00000636940.1:n.3108A>T
ENST00000637015.1:c.2479A>T
ENST00000637568.1:c.2393A>T
ENST00000637741.1:n.1777A>T
ENST00000637810.1:c.2453A>T	ENSP00000489636.1:p.Gln818Leu
ENST00000637904.1:c.2612A>T	ENSP00000490550.1:p.Gln871Leu
ENST00000647938.1:c.4742A>T	ENSP00000498155.1:p.Gln1581Leu
ENST00000346085.9:c.4742A>T	ENSP00000344546.4:p.Gln1581Leu
ENST00000350026.9:c.4703A>T	ENSP00000055163.7:p.Gln1568Leu
ENST00000414678.6:c.3269A>T	ENSP00000412835.2:p.Gln1090Leu
NM_017519.2:c.4703A>T	NP_059989.2:p.Gln1568Leu
NM_020732.3:c.4742A>T	NP_065783.3:p.Gln1581Leu
XM_005267069.3:c.4862A>T	XP_005267126.2:p.Gln1621Leu
XM_011535984.1:c.3941A>T	XP_011534286.1:p.Gln1314Leu
XM_011535985.1:c.3761A>T	XP_011534287.1:p.Gln1254Leu
XM_011535986.1:c.3521A>T	XP_011534288.1:p.Gln1174Leu
XM_011535987.1:c.3140A>T	XP_011534289.1:p.Gln1047Leu
XM_011535988.1:c.2003A>T	XP_011534290.1:p.Gln668Leu
NM_001346813.1:c.4862A>T	NP_001333742.1:p.Gln1621Leu
NM_001363725.1:c.2612A>T	NP_001350654.1:p.Gln871Leu
XM_011535984.2:c.5072A>T	XP_011534286.2:p.Gln1691Leu
XM_011535988.3:c.2003A>T	XP_011534290.1:p.Gln668Leu
XM_017011103.2:c.4973A>T	XP_016866592.1:p.Gln1658Leu
XM_017011104.1:c.4943A>T	XP_016866593.1:p.Gln1648Leu
XM_017011105.2:c.4913A>T	XP_016866594.1:p.Gln1638Leu
XM_017011106.2:c.4784A>T	XP_016866595.1:p.Gln1595Leu
XM_017011107.2:c.4763A>T	XP_016866596.1:p.Gln1588Leu
XR_002956289.1:n.5058A>T
NM_001363725.2:c.2612A>T	NP_001350654.1:p.Gln871Leu
NM_001371656.1:c.4991A>T	NP_001358585.1:p.Gln1664Leu
NM_001374820.1:c.4991A>T	NP_001361749.1:p.Gln1664Leu
NM_001374828.1:c.5111A>T MANE Select	NP_001361757.1:p.Gln1704Leu
NM_017519.3:c.4952A>T	NP_059989.3:p.Gln1651Leu